SU604499A3 - Способ получени галоидированных эфирохлорангидридов кислот фосфора - Google Patents

Способ получени галоидированных эфирохлорангидридов кислот фосфора

Info

Publication number: SU604499A3
Authority: SU; USSR - Soviet Union
Prior art keywords: chlorine; acid; theory; chloride; phosphoric acid
Prior art date: 1975-02-22

Application number

SU762325907A

Other languages

English (en)

Russian (ru)

Inventor

Арлт Дитер

Original Assignee

Байер Аг., (Фирма)

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1975-02-22

Filing date

1976-02-20

Publication date

1978-04-25

1976-02-20 Application filed by Байер Аг., (Фирма) filed Critical Байер Аг., (Фирма)

1978-04-25 Application granted granted Critical

1978-04-25 Publication of SU604499A3 publication Critical patent/SU604499A3/ru

Links

238000000034 method Methods 0.000 title claims 4
150000003017 phosphorus Chemical class 0.000 title claims 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N phosphoric acid Substances OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 18
229910052801 chlorine Inorganic materials 0.000 claims 14
239000000460 chlorine Substances 0.000 claims 14
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 13
229910000147 aluminium phosphate Inorganic materials 0.000 claims 11
238000004508 fractional distillation Methods 0.000 claims 7
150000002148 esters Chemical class 0.000 claims 6
XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 claims 6
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims 5
239000002253 acid Substances 0.000 claims 5
238000006243 chemical reaction Methods 0.000 claims 5
238000001816 cooling Methods 0.000 claims 5
-1 1,2-dichloroethyl Chemical group 0.000 claims 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 4
229910052794 bromium Inorganic materials 0.000 claims 4
229910021578 Iron(III) chloride Inorganic materials 0.000 claims 3
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 3
238000004821 distillation Methods 0.000 claims 3
239000007789 gas Substances 0.000 claims 3
RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 claims 3
239000000203 mixture Substances 0.000 claims 3
229910052698 phosphorus Inorganic materials 0.000 claims 3
239000011574 phosphorus Substances 0.000 claims 3
238000003756 stirring Methods 0.000 claims 3
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
238000005727 Friedel-Crafts reaction Methods 0.000 claims 2
150000001336 alkenes Chemical class 0.000 claims 2
VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims 2
150000001875 compounds Chemical class 0.000 claims 2
229910052731 fluorine Inorganic materials 0.000 claims 2
239000011737 fluorine Substances 0.000 claims 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 claims 2
YLGYEVGIVHHPKT-UHFFFAOYSA-N 1,2-dichloroethyl dihydrogen phosphate Chemical compound OP(O)(=O)OC(Cl)CCl YLGYEVGIVHHPKT-UHFFFAOYSA-N 0.000 claims 1
DEWLEGDTCGBNGU-UHFFFAOYSA-N 1,3-dichloropropan-2-ol Chemical compound ClCC(O)CCl DEWLEGDTCGBNGU-UHFFFAOYSA-N 0.000 claims 1
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 claims 1
ZNFMTXVCNCJLNM-UHFFFAOYSA-N 2-chloro-1-(2-chloro-1-fluoroethoxy)-1-fluoroethane Chemical class ClCC(F)OC(F)CCl ZNFMTXVCNCJLNM-UHFFFAOYSA-N 0.000 claims 1
VKEIPALYOJMDAC-UHFFFAOYSA-N 3,3,3-trichloroprop-1-ene Chemical compound ClC(Cl)(Cl)C=C VKEIPALYOJMDAC-UHFFFAOYSA-N 0.000 claims 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims 1
150000007513 acids Chemical class 0.000 claims 1
238000009835 boiling Methods 0.000 claims 1
INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 claims 1
239000003054 catalyst Substances 0.000 claims 1
UETQVDZZPKAQIC-UHFFFAOYSA-N chlorane Chemical compound Cl.Cl.Cl.Cl UETQVDZZPKAQIC-UHFFFAOYSA-N 0.000 claims 1
125000001309 chloro group Chemical group Cl* 0.000 claims 1
HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 claims 1
238000000354 decomposition reaction Methods 0.000 claims 1
SNVCRNWSNUUGEA-UHFFFAOYSA-N dichlorophosphoryloxymethane Chemical compound COP(Cl)(Cl)=O SNVCRNWSNUUGEA-UHFFFAOYSA-N 0.000 claims 1
YBBUMZUSUMRUKT-UHFFFAOYSA-N dimethyl hydrogen phosphate hydrochloride Chemical compound Cl.COP(O)(=O)OC YBBUMZUSUMRUKT-UHFFFAOYSA-N 0.000 claims 1
229960003750 ethyl chloride Drugs 0.000 claims 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
125000005843 halogen group Chemical group 0.000 claims 1
239000001257 hydrogen Substances 0.000 claims 1
229910052739 hydrogen Inorganic materials 0.000 claims 1
238000004519 manufacturing process Methods 0.000 claims 1
SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 claims 1
239000003921 oil Substances 0.000 claims 1
150000003254 radicals Chemical class 0.000 claims 1
239000011541 reaction mixture Substances 0.000 claims 1
238000005292 vacuum distillation Methods 0.000 claims 1
235000005074 zinc chloride Nutrition 0.000 claims 1
239000011592 zinc chloride Substances 0.000 claims 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/14—Esters of phosphoric acids containing P(=O)-halide groups

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Biochemistry (AREA)
General Health & Medical Sciences (AREA)
Molecular Biology (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

SU762325907A 1975-02-22 1976-02-20 Способ получени галоидированных эфирохлорангидридов кислот фосфора SU604499A3 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE2507779A DE2507779C2 (de)	1975-02-22	1975-02-22	Phosphorsäureesterhalogenide sowie Verfahren zu deren Herstellung

Publications (1)

Publication Number	Publication Date
SU604499A3 true SU604499A3 (ru)	1978-04-25

Family

ID=5939608

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU762325907A SU604499A3 (ru)	1975-02-22	1976-02-20	Способ получени галоидированных эфирохлорангидридов кислот фосфора

Country Status (22)

Country	Link
JP (1)	JPS5910677B2 (de)
AT (1)	AT341543B (de)
BE (1)	BE838737A (de)
BR (1)	BR7601096A (de)
CA (1)	CA1072574A (de)
CH (1)	CH623058A5 (de)
CS (1)	CS181696B2 (de)
DD (1)	DD125577A5 (de)
DE (1)	DE2507779C2 (de)
DK (1)	DK141936C (de)
ES (1)	ES445370A1 (de)
FR (1)	FR2301531A1 (de)
GB (1)	GB1513341A (de)
HU (1)	HU175203B (de)
IL (1)	IL49077A (de)
IT (1)	IT1053874B (de)
LU (1)	LU74395A1 (de)
NL (1)	NL187355C (de)
PL (1)	PL99859B1 (de)
RO (1)	RO68979A (de)
SU (1)	SU604499A3 (de)
ZA (1)	ZA761006B (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2630561A1 (de) *	1976-07-07	1978-01-19	Bayer Ag	1-fluor-2-halogen-aethyl-thionophosphor (phosphon)-saeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide, akarizide und nematizide

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IL30533A (en) *	1967-09-01	1972-01-27	Bayer Ag	Thiol-or thionothiol-phosphoric or-phosphonic acid esters
DE2417143C2 (de) *	1974-04-09	1982-04-15	Bayer Ag, 5090 Leverkusen	Verfahren zur Herstellung von (Thio) Phosphor(Phosphon)säureestern

1975
- 1975-02-22 DE DE2507779A patent/DE2507779C2/de not_active Expired
1976
- 1976-01-21 HU HU76BA3358A patent/HU175203B/hu unknown
- 1976-02-18 CH CH200576A patent/CH623058A5/de not_active IP Right Cessation
- 1976-02-19 RO RO7684853A patent/RO68979A/ro unknown
- 1976-02-19 NL NLAANVRAGE7601697,A patent/NL187355C/xx not_active IP Right Cessation
- 1976-02-20 FR FR7604795A patent/FR2301531A1/fr active Granted
- 1976-02-20 PL PL1976187346A patent/PL99859B1/pl unknown
- 1976-02-20 BE BE2054842A patent/BE838737A/xx not_active IP Right Cessation
- 1976-02-20 IT IT48195/76A patent/IT1053874B/it active
- 1976-02-20 SU SU762325907A patent/SU604499A3/ru active
- 1976-02-20 DD DD191380A patent/DD125577A5/xx unknown
- 1976-02-20 GB GB6791/76A patent/GB1513341A/en not_active Expired
- 1976-02-20 ES ES445370A patent/ES445370A1/es not_active Expired
- 1976-02-20 IL IL7649077A patent/IL49077A/xx unknown
- 1976-02-20 ZA ZA761006A patent/ZA761006B/xx unknown
- 1976-02-20 CS CS7600001144A patent/CS181696B2/cs unknown
- 1976-02-20 DK DK70576A patent/DK141936C/da not_active IP Right Cessation
- 1976-02-20 AT AT122076A patent/AT341543B/de not_active IP Right Cessation
- 1976-02-20 BR BR7601096A patent/BR7601096A/pt unknown
- 1976-02-20 CA CA246,203A patent/CA1072574A/en not_active Expired
- 1976-02-20 LU LU74395A patent/LU74395A1/xx unknown
- 1976-02-20 JP JP51017191A patent/JPS5910677B2/ja not_active Expired

Also Published As

Publication number	Publication date
FR2301531A1 (fr)	1976-09-17
ATA122076A (de)	1977-06-15
PL99859B1 (pl)	1978-08-31
DK141936B (da)	1980-07-21
DD125577A5 (de)	1977-05-04
ZA761006B (en)	1977-02-23
AU1130776A (en)	1977-08-25
FR2301531B1 (de)	1980-11-21
AT341543B (de)	1978-02-10
NL187355C (nl)	1991-09-02
RO68979A (ro)	1981-05-30
CS181696B2 (en)	1978-03-31
DK70576A (da)	1976-08-23
DK141936C (da)	1980-12-01
JPS51110521A (de)	1976-09-30
HU175203B (hu)	1980-06-28
IL49077A (en)	1979-07-25
DE2507779C2 (de)	1982-07-01
ES445370A1 (es)	1977-07-01
IT1053874B (it)	1981-10-10
CA1072574A (en)	1980-02-26
CH623058A5 (en)	1981-05-15
JPS5910677B2 (ja)	1984-03-10
BR7601096A (pt)	1976-09-14
IL49077A0 (en)	1976-04-30
DE2507779A1 (de)	1976-09-02
NL7601697A (nl)	1976-08-24
GB1513341A (en)	1978-06-07
BE838737A (fr)	1976-08-20
NL187355B (nl)	1991-04-02
LU74395A1 (de)	1977-01-06

Publication	Publication Date	Title
US3812222A (en)	1974-05-21	Process for the manufacture of alkane phosphonic acid diesters
US4377537A (en)	1983-03-22	Preparation of alkane phosphonic and phosphinic acid aryl esters
SU609471A3 (ru)	1978-05-30	Способ получени эфиров кислот фосфора
US3787486A (en)	1974-01-22	Preparation of haloethane phosphonic acids
JP6826110B2 (ja)	2021-02-03	ホスフィネート類を製造する方法
SU604499A3 (ru)	1978-04-25	Способ получени галоидированных эфирохлорангидридов кислот фосфора
CA1110649A (en)	1981-10-13	Process for the preparation of four-membered cyclic ketones
US5177238A (en)	1993-01-05	Preparation of dialkyl allylphosphonic acid diesters
US2968667A (en)	1961-01-17	Bis (perfluoroalkylmethyl) sulfites and their preparation
US7435841B2 (en)	2008-10-14	Preparation of halohydrocarbyl phosphonic acid diesters
US2806049A (en)	1957-09-10	Halo-substituted organo-phosphorous compounds
JPH0853479A (ja)	1996-02-27	ホスホン酸エステル及び該化合物の製法
US5017719A (en)	1991-05-21	Esters of arylbisperfluoroalkylcarbinols, and a process for the preparation of these compounds
EP1685141B1 (de)	2010-01-06	Verfahren zur herstellung von alkylphenylphosphaten
US4478763A (en)	1984-10-23	Process for preparing alpha-fluorinated alkanediphosphonates
US3272892A (en)	1966-09-13	Method of preparing organic phosphonates by transesterification
US4182733A (en)	1980-01-08	Process for preparing phosphoric acid esterhalides
SU1490123A1 (ru)	1989-06-30	Способ получени эфирофторангидридов алкилфосфонистых кислот
US3505433A (en)	1970-04-07	2-haloperfluoro-1-cycloalken-1-ylphosphoryl compounds
US5717128A (en)	1998-02-10	Preparation of alkylesters of 0,0-dialkyl-4-phosphono-2-methyl-2-butenoic acid and alkyl esters of 4-halo-2-methyl-2-butenoic acid containing a high percentage of E isomers
SU734213A1 (ru)	1980-05-15	Способ получени диалкиловых эфиров замещенных этинилфосфоновых кислот
US3525678A (en)	1970-08-25	Method of preparing dialkyl esters of perfluorodicarboxylic acids
DK149471B (da)	1986-06-23	Fremgangsmaade til fremstilling af phosphorsyrealkylesterdichlorider
US4454072A (en)	1984-06-12	Process for the preparation of ω-fluorosulfatoperfluoroalkanoic acid derivatives
US4138452A (en)	1979-02-06	Process for preparing phosphoric acid esterhalides