CN106008575B - 一种频哪醇硼烷的制备方法 - Google Patents
一种频哪醇硼烷的制备方法 Download PDFInfo
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- CN106008575B CN106008575B CN201610373740.9A CN201610373740A CN106008575B CN 106008575 B CN106008575 B CN 106008575B CN 201610373740 A CN201610373740 A CN 201610373740A CN 106008575 B CN106008575 B CN 106008575B
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- pinacol
- borine
- condensation reaction
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- IVDFJHOHABJVEH-UHFFFAOYSA-N pinacol Chemical compound CC(C)(O)C(C)(C)O IVDFJHOHABJVEH-UHFFFAOYSA-N 0.000 title claims abstract description 124
- 229910000085 borane Inorganic materials 0.000 title claims abstract description 42
- UORVGPXVDQYIDP-UHFFFAOYSA-N trihydridoboron Substances B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 title claims abstract description 42
- 238000002360 preparation method Methods 0.000 title claims abstract description 27
- 238000006482 condensation reaction Methods 0.000 claims abstract description 20
- 238000000034 method Methods 0.000 claims abstract description 19
- UOALEFQKAOQICC-UHFFFAOYSA-N chloroborane Chemical class ClB UOALEFQKAOQICC-UHFFFAOYSA-N 0.000 claims abstract description 14
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical group ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 27
- 238000006243 chemical reaction Methods 0.000 claims description 24
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical group CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 18
- 229910052757 nitrogen Inorganic materials 0.000 claims description 17
- 150000007530 organic bases Chemical class 0.000 claims description 14
- 238000003756 stirring Methods 0.000 claims description 11
- 239000003960 organic solvent Substances 0.000 claims description 10
- 239000007787 solid Substances 0.000 claims description 9
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 7
- QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical compound CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 claims description 6
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 5
- 238000000926 separation method Methods 0.000 claims description 3
- 238000009833 condensation Methods 0.000 claims description 2
- 230000005494 condensation Effects 0.000 claims description 2
- 238000010792 warming Methods 0.000 claims description 2
- LHCGBIFHSCCRRG-UHFFFAOYSA-N dichloroborane Chemical compound ClBCl LHCGBIFHSCCRRG-UHFFFAOYSA-N 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- -1 hydrogen furans Chemical class 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 7
- 239000002994 raw material Substances 0.000 abstract description 5
- 239000000126 substance Substances 0.000 abstract description 5
- 238000010189 synthetic method Methods 0.000 abstract description 4
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
- 238000003786 synthesis reaction Methods 0.000 abstract description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 30
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 11
- GKWKOCYSCDZTAX-UHFFFAOYSA-N dichloroboron Chemical compound Cl[B]Cl GKWKOCYSCDZTAX-UHFFFAOYSA-N 0.000 description 11
- 239000000047 product Substances 0.000 description 9
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 7
- 230000006837 decompression Effects 0.000 description 6
- 239000000706 filtrate Substances 0.000 description 6
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 3
- 125000003963 dichloro group Chemical group Cl* 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- CMEWLCATCRTSGF-UHFFFAOYSA-N N,N-dimethyl-4-nitrosoaniline Chemical compound CN(C)C1=CC=C(N=O)C=C1 CMEWLCATCRTSGF-UHFFFAOYSA-N 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000001345 alkine derivatives Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000001502 aryl halides Chemical class 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000006197 hydroboration reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical class ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 description 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
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/022—Boron compounds without C-boron linkages
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Abstract
Description
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CN201610373740.9A CN106008575B (zh) | 2016-05-30 | 2016-05-30 | 一种频哪醇硼烷的制备方法 |
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CN201610373740.9A CN106008575B (zh) | 2016-05-30 | 2016-05-30 | 一种频哪醇硼烷的制备方法 |
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CN106008575A CN106008575A (zh) | 2016-10-12 |
CN106008575B true CN106008575B (zh) | 2018-01-30 |
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Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104086576A (zh) * | 2014-07-18 | 2014-10-08 | 上海格物致知医药科技有限公司 | 高纯度硼烷气体的制备方法及该硼烷气体的应用 |
CN105524099A (zh) * | 2016-01-12 | 2016-04-27 | 沧州普瑞东方科技有限公司 | 一种制备联硼酸酯的工艺 |
-
2016
- 2016-05-30 CN CN201610373740.9A patent/CN106008575B/zh active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104086576A (zh) * | 2014-07-18 | 2014-10-08 | 上海格物致知医药科技有限公司 | 高纯度硼烷气体的制备方法及该硼烷气体的应用 |
CN105524099A (zh) * | 2016-01-12 | 2016-04-27 | 沧州普瑞东方科技有限公司 | 一种制备联硼酸酯的工艺 |
Non-Patent Citations (8)
Title |
---|
Facile hydroboration of (Z)-1-trimethylsilyl-1-alkenes with dichloroborane–dioxane complex: An easy access to gem-dimetalloalkanes containing boron and silicon;Narayan G. Bhat et al;《Journal of Organometallic Chemistry》;20060123;第691 卷;第1298-1300页 * |
Mild and Stereoselective Hydroborations of Functionalized Alkynes and Alkenes Using Pinacolborane;Charles E. Tucker et al;《J. Org. Chem.》;19921201;第57卷;第3482-3485页 * |
Novel Matrix Metallo-Proteinase (MMP-2) Phosphonoboronate Inhibitors;Inna Pergament et al;《Bioorganic & Medicinal ChemistryLetters》;20021231;第12卷;第1215-1218页 * |
Organoboranes.30. Convenient Procedures for the Synthesis of Alkyl-and Alkenylboronic Acids and Esters;Herbert C. Brown et al;《Organometallics》;19831231;第2卷;第1311-1316页 * |
Practical synthesis of pinacolborane for one-pot synthesis of unsymmetrical biaryls via aromatic C–H borylation–cross-coupling sequence;Takao Kikuchi et al;《Tetrahedron》;20080403;第64卷;第4967–4971页 * |
Regioselective electrophilic borylation of haloarenes;Alessandro Del Grosso et al;《ChemComm》;20150105;第51卷;第2878-2881页 * |
simple synthesis of B-2-(1-trimethylgermyl-1-alkyl)-1,3,2-dioxaborinanes. Isolation and selective oxidation to 1-trimethylgermyl-1-alkanols;Narayan G. Bhat et al;《Tetrahedron Letters》;20050706;第46卷;第5647-5649页 * |
The Influence of Boryl Substituents on the Formation and Reactivity of Adjacent and Vicinal Free Radical Centers;John C. Walton et al;《J. Am. Chem. Soc.》;20000523;第122卷;第5455-5463页 * |
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CN106008575A (zh) | 2016-10-12 |
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Effective date of registration: 20240622 Address after: 300192 Tianjin Science and Technology Square 6-1204 (Tiankai Park), west of Science and Technology East Road, Nankai District, Tianjin Patentee after: Tianjin Tiankai Yunlai Co.,Ltd. Country or region after: China Address before: 122500 Chaoyang Economic Development Zone, Chaoyang County, Chaoyang City, Liaoning Province Patentee before: CHAOYANG KANGQUAN MEDICAL TECHNOLOGY Co.,Ltd. Country or region before: China |