NO754162L - - Google Patents

Info

Publication number
NO754162L
NO754162L NO754162A NO754162A NO754162L NO 754162 L NO754162 L NO 754162L NO 754162 A NO754162 A NO 754162A NO 754162 A NO754162 A NO 754162A NO 754162 L NO754162 L NO 754162L
Authority
NO
Norway
Prior art keywords
formula
pyrolysis
alkyl
alkaline earth
earth metal
Prior art date
Application number
NO754162A
Other languages
English (en)
Inventor
G Cipriani
C Neri
Original Assignee
Anic Spa
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.)
Filing date
Publication date
Application filed by Anic Spa filed Critical Anic Spa
Publication of NO754162L publication Critical patent/NO754162L/no

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/28Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/30Oxygen or sulfur atoms
    • C07D233/32One oxygen atom
    • C07D233/34Ethylene-urea
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C273/00Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C273/18Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas
    • C07C273/1809Preparation of urea or its derivatives, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups of substituted ureas with formation of the N-C(O)-N moiety
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/28Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/30Oxygen or sulfur atoms
    • C07D233/32One oxygen atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/06Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D239/08Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms directly attached in position 2
    • C07D239/10Oxygen or sulfur atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

Foreliggende oppfinnelse vedrorer en fremgangsmåte for fremstilling av urinstoff-derivater med formel: hvori N = 2, 3 eller 4 og R og R<1>hver er hydrogen, alkyl eller aryl, cycloalkyl, aralkyl eller alkahyl, den substituert eller usubstituert, mettet eller umettet, ved pyrolyse av tilsvarende karbarnater med formel:
hvori Me er et alkalmetall eller et jordalkalimetall.
Slike karbamater fremstilles fordelaktig ved en fremgangsmåte som angitt i ansokning 75/4161.
Pyrolysen foregår i henhold til fSigende reaksjonsskjema:
ved en temperatur mellom 150 og 400°C ved omgivelsenes trykk eller foretrukket under underatmosfærisk trykk. Under disse betingelser destilerer eller sublemerer urinstoffderivatet.
Eksempel 1
20 g CgHj-NH-COOLi anbringes i et forsoksror med forlengelsesror for innsetting i en elektrisk ovn og hvori der er et vakuum på
20 mm kvikksolv (absolutt trykk).
Ovnen oppvarmes til 300°C og på veggene av forsoksroret sublimerer 14 g bifenylurinstof f f "idet resten utgjores av 6 g Li^CO-. ut* au^oaæ.
to.
Eksempel 2
behandles som ovenfor ved 350°C dg forer til 9 g n\ - • dimetyletylenurinstoff og en rest på 11 gK2C03. /^ oIo^ l sjMj^ Ui a*, iroxkju^ oi ( fimx& A<$* Å ,
PATENTKRAV
1. Fremgangsmåte for syntese av urinstoff-derivater valgt fra gruppen med formel:
hvor n = 2, 3 eller 4 og R og R<1>er hydrogen, alkyl, aryl,cycloalkyl, aralkyl eller alkaryl, enten substituert eller usubstituert og enten mettet eller umettet, ved pyrolyse av tilsvarende karbarnater med formel:
eller
hvori Me er et alkalimetall elleret-jordalkalimetall.
2. Fremgangsmåte som angitt i krav 1,
karakterisert vedat pyrolysen gjennomfores ved en temperatur mellom 150 og 400°C.

Claims (1)

  1. Fremgangsmåte for fremstilling av karbamider med formel
    hvori n er 2, 3 eller 4, R <1> er fenyl og R" er alkyl, karakterisert ved at et karbamat med formelen
    eller
    hvori R, R' og R" har den ovennevnte betydning og Me er et alkali- eller et jordalkali-metall, underkastes pyrolyse ved temperatur mellom 150 og 400°C.
NO754162A 1974-12-10 1975-12-09 NO754162L (no)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IT30341/74A IT1026907B (it) 1974-12-10 1974-12-10 Procedimento per la sintesi di uree

Publications (1)

Publication Number Publication Date
NO754162L true NO754162L (no) 1976-06-11

Family

ID=11229569

Family Applications (1)

Application Number Title Priority Date Filing Date
NO754162A NO754162L (no) 1974-12-10 1975-12-09

Country Status (19)

Country Link
US (1) US4063021A (no)
JP (1) JPS594423B2 (no)
AT (1) AT349487B (no)
BE (1) BE836387A (no)
CA (1) CA1058174A (no)
CH (1) CH624097A5 (no)
DE (1) DE2555582A1 (no)
DK (1) DK557075A (no)
ES (1) ES443591A1 (no)
FR (1) FR2294169A1 (no)
GB (1) GB1499180A (no)
IE (1) IE42456B1 (no)
IT (1) IT1026907B (no)
LU (1) LU73953A1 (no)
NL (1) NL172951C (no)
NO (1) NO754162L (no)
SE (1) SE431203B (no)
SU (1) SU900804A3 (no)
ZA (1) ZA757617B (no)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57139069A (en) * 1981-02-20 1982-08-27 Nippon Tokushu Noyaku Seizo Kk Substituted tetrahydropyrimidinone derivative, its preparation and herbicide
US4405794A (en) * 1981-12-18 1983-09-20 The Dow Chemical Company Preparation of 2-oxazolidinone and ethyleneurea
JPS58140078A (ja) * 1982-02-16 1983-08-19 Nippon Tokushu Noyaku Seizo Kk メチル置換テトラヒドロ−2−ピリミジノン誘導体、その製法、その中間体及び該中間体の製法、並びに除草剤
JPH0333420U (no) * 1989-08-10 1991-04-02
DE19743760A1 (de) * 1997-10-02 1999-04-08 Basf Ag Verfahren zur Herstellung von cyclischen Harnstoffderivaten
DE29820895U1 (de) 1998-11-23 1999-02-18 ECS Eich Maschinenbau GmbH, 35745 Herborn Mobiles Wasserreinigungsgerät

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2276696A (en) * 1939-10-06 1942-03-17 Sharples Chemicals Inc Manufacture of homologues of urea
US3053891A (en) * 1959-05-05 1962-09-11 Chemical Construction Corp Process for production of urea
US3923833A (en) * 1968-05-01 1975-12-02 Hoffmann La Roche N-{8 (1-cyano-2-phenyl)ethyl{9 carbamates

Also Published As

Publication number Publication date
IE42456L (en) 1976-06-10
US4063021A (en) 1977-12-13
DE2555582A1 (de) 1976-06-16
SE7513879L (sv) 1976-06-11
NL172951C (nl) 1983-11-16
SU900804A3 (ru) 1982-01-23
DK557075A (da) 1976-06-11
CA1058174A (en) 1979-07-10
ES443591A1 (es) 1977-05-01
NL7514362A (nl) 1976-06-14
JPS5182225A (no) 1976-07-19
NL172951B (nl) 1983-06-16
AT349487B (de) 1979-04-10
JPS594423B2 (ja) 1984-01-30
ATA933175A (de) 1978-09-15
ZA757617B (en) 1976-11-24
IE42456B1 (en) 1980-08-13
FR2294169A1 (fr) 1976-07-09
BE836387A (fr) 1976-06-08
GB1499180A (en) 1978-01-25
LU73953A1 (no) 1976-07-01
IT1026907B (it) 1978-10-20
FR2294169B1 (no) 1982-05-28
SE431203B (sv) 1984-01-23
CH624097A5 (no) 1981-07-15

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