JPS6232755B2 - - Google Patents
Info
- Publication number
- JPS6232755B2 JPS6232755B2 JP57046481A JP4648182A JPS6232755B2 JP S6232755 B2 JPS6232755 B2 JP S6232755B2 JP 57046481 A JP57046481 A JP 57046481A JP 4648182 A JP4648182 A JP 4648182A JP S6232755 B2 JPS6232755 B2 JP S6232755B2
- Authority
- JP
- Japan
- Prior art keywords
- borane
- chem
- compound
- benzene
- general formula
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 claims description 16
- 229910000085 borane Inorganic materials 0.000 claims description 10
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 4
- 229910052717 sulfur Chemical group 0.000 claims description 4
- 239000002879 Lewis base Substances 0.000 claims description 3
- 239000012298 atmosphere Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 125000004434 sulfur atom Chemical group 0.000 claims description 3
- 125000002619 bicyclic group Chemical group 0.000 claims description 2
- 230000007935 neutral effect Effects 0.000 claims description 2
- YPWFISCTZQNZAU-UHFFFAOYSA-N Thiane Chemical compound C1CCSCC1 YPWFISCTZQNZAU-UHFFFAOYSA-N 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 30
- 150000001875 compounds Chemical class 0.000 description 22
- 238000000034 method Methods 0.000 description 10
- 239000007787 solid Substances 0.000 description 10
- 238000006197 hydroboration reaction Methods 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 230000003287 optical effect Effects 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 5
- 238000004458 analytical method Methods 0.000 description 5
- WQADWIOXOXRPLN-UHFFFAOYSA-N 1,3-dithiane Chemical compound C1CSCSC1 WQADWIOXOXRPLN-UHFFFAOYSA-N 0.000 description 4
- BKOOMYPCSUNDGP-UHFFFAOYSA-N 2-methylbut-2-ene Chemical compound CC=C(C)C BKOOMYPCSUNDGP-UHFFFAOYSA-N 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- JQWHASGSAFIOCM-UHFFFAOYSA-M sodium periodate Chemical compound [Na+].[O-]I(=O)(=O)=O JQWHASGSAFIOCM-UHFFFAOYSA-M 0.000 description 4
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000003638 chemical reducing agent Substances 0.000 description 3
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000006140 methanolysis reaction Methods 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 238000003822 preparative gas chromatography Methods 0.000 description 3
- CTMHWPIWNRWQEG-UHFFFAOYSA-N 1-methylcyclohexene Chemical compound CC1=CCCCC1 CTMHWPIWNRWQEG-UHFFFAOYSA-N 0.000 description 2
- WAPNOHKVXSQRPX-UHFFFAOYSA-N 1-phenylethanol Chemical compound CC(O)C1=CC=CC=C1 WAPNOHKVXSQRPX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- XPNGNIFUDRPBFJ-UHFFFAOYSA-N alpha-methylbenzylalcohol Natural products CC1=CC=CC=C1CO XPNGNIFUDRPBFJ-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- UORVGPXVDQYIDP-BJUDXGSMSA-N borane Chemical class [10BH3] UORVGPXVDQYIDP-BJUDXGSMSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000007363 ring formation reaction Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- KMRMUZKLFIEVAO-IUCAKERBSA-N (1s,5r)-6,6-dimethylbicyclo[3.1.1]hept-3-ene-4-carbaldehyde Chemical compound C1[C@@H]2C(C)(C)[C@H]1CC=C2C=O KMRMUZKLFIEVAO-IUCAKERBSA-N 0.000 description 1
- BVOMRRWJQOJMPA-UHFFFAOYSA-N 1,2,3-trithiane Chemical compound C1CSSSC1 BVOMRRWJQOJMPA-UHFFFAOYSA-N 0.000 description 1
- LORRLQMLLQLPSJ-UHFFFAOYSA-N 1,3,5-Trithiane, Natural products C1SCSCS1 LORRLQMLLQLPSJ-UHFFFAOYSA-N 0.000 description 1
- JICAHGJPTZDVCA-UHFFFAOYSA-N B.S1(CSCCC1)=O Chemical compound B.S1(CSCCC1)=O JICAHGJPTZDVCA-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- PDSNLYSELAIEBU-UHFFFAOYSA-N Longifolene Chemical compound C1CCC(C)(C)C2C3CCC2C1(C)C3=C PDSNLYSELAIEBU-UHFFFAOYSA-N 0.000 description 1
- ZPUKHRHPJKNORC-UHFFFAOYSA-N Longifolene Natural products CC1(C)CCCC2(C)C3CCC1(C3)C2=C ZPUKHRHPJKNORC-UHFFFAOYSA-N 0.000 description 1
- KMRMUZKLFIEVAO-RKDXNWHRSA-N Myrtenal Natural products C1[C@H]2C(C)(C)[C@@H]1CC=C2C=O KMRMUZKLFIEVAO-RKDXNWHRSA-N 0.000 description 1
- RXBQNMWIQKOSCS-UHFFFAOYSA-N Myrthenol Natural products C1C2C(C)(C)C1CC=C2CO RXBQNMWIQKOSCS-UHFFFAOYSA-N 0.000 description 1
- RXBQNMWIQKOSCS-IUCAKERBSA-N [(1s,5r)-6,6-dimethyl-4-bicyclo[3.1.1]hept-3-enyl]methanol Chemical compound C1[C@@H]2C(C)(C)[C@H]1CC=C2CO RXBQNMWIQKOSCS-IUCAKERBSA-N 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- ZOCHARZZJNPSEU-UHFFFAOYSA-N diboron Chemical compound B#B ZOCHARZZJNPSEU-UHFFFAOYSA-N 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000012280 lithium aluminium hydride Substances 0.000 description 1
- -1 lithium aluminum hydride Chemical compound 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 238000004452 microanalysis Methods 0.000 description 1
- 208000022961 microcephaly, developmental delay, and brittle hair syndrome Diseases 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000001979 organolithium group Chemical group 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- ZJLMKPKYJBQJNH-UHFFFAOYSA-N propane-1,3-dithiol Chemical compound SCCCS ZJLMKPKYJBQJNH-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011946 reduction process Methods 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D339/00—Heterocyclic compounds containing rings having two sulfur atoms as the only ring hetero atoms
- C07D339/08—Six-membered rings
-
- 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
- C07F5/027—Organoboranes and organoborohydrides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D341/00—Heterocyclic compounds containing rings having three or more sulfur atoms as the only ring hetero atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8109392 | 1981-03-25 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS57206689A JPS57206689A (en) | 1982-12-18 |
| JPS6232755B2 true JPS6232755B2 (OSRAM) | 1987-07-16 |
Family
ID=10520658
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57046481A Granted JPS57206689A (en) | 1981-03-25 | 1982-03-25 | Novel chiral organoborans and manufacture |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US4436919A (OSRAM) |
| EP (1) | EP0061408B1 (OSRAM) |
| JP (1) | JPS57206689A (OSRAM) |
| KR (1) | KR860000588B1 (OSRAM) |
| AR (1) | AR227966A1 (OSRAM) |
| AT (1) | ATE11292T1 (OSRAM) |
| AU (1) | AU547100B2 (OSRAM) |
| CA (1) | CA1190936A (OSRAM) |
| DE (1) | DE3261902D1 (OSRAM) |
| DK (1) | DK158583C (OSRAM) |
| FI (1) | FI68240C (OSRAM) |
| MX (1) | MX7053E (OSRAM) |
| NO (1) | NO155441C (OSRAM) |
| NZ (1) | NZ200034A (OSRAM) |
| PL (1) | PL130111B1 (OSRAM) |
| ZA (1) | ZA821644B (OSRAM) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NZ221032A (en) * | 1986-07-15 | 1990-02-26 | Nihon Nohyaku Co Ltd | 1,3,5 trithiane derivatives and pharmaceutical compositions |
| FR2749847B1 (fr) * | 1996-06-13 | 1998-11-06 | Expansia Sa | Organoboranes chiraux |
| HRP20241104T1 (hr) | 2011-04-12 | 2024-11-08 | Välinge Innovation AB | Postupak proizvodnje sloja |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3254129A (en) * | 1961-01-17 | 1966-05-31 | Herbert C Brown | Optically active organoboranes |
-
1982
- 1982-03-11 ZA ZA821644A patent/ZA821644B/xx unknown
- 1982-03-17 US US06/358,847 patent/US4436919A/en not_active Expired - Lifetime
- 1982-03-17 NZ NZ200034A patent/NZ200034A/en unknown
- 1982-03-17 AR AR288784A patent/AR227966A1/es active
- 1982-03-19 FI FI820970A patent/FI68240C/fi not_active IP Right Cessation
- 1982-03-23 NO NO820963A patent/NO155441C/no unknown
- 1982-03-24 KR KR8201248A patent/KR860000588B1/ko not_active Expired
- 1982-03-24 CA CA000399275A patent/CA1190936A/en not_active Expired
- 1982-03-24 MX MX829990U patent/MX7053E/es unknown
- 1982-03-24 DK DK132782A patent/DK158583C/da not_active IP Right Cessation
- 1982-03-24 AU AU81864/82A patent/AU547100B2/en not_active Ceased
- 1982-03-24 AT AT82400529T patent/ATE11292T1/de active
- 1982-03-24 DE DE8282400529T patent/DE3261902D1/de not_active Expired
- 1982-03-24 EP EP82400529A patent/EP0061408B1/fr not_active Expired
- 1982-03-24 PL PL1982235608A patent/PL130111B1/pl unknown
- 1982-03-25 JP JP57046481A patent/JPS57206689A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| NZ200034A (en) | 1985-01-31 |
| EP0061408A1 (fr) | 1982-09-29 |
| FI68240C (fi) | 1985-08-12 |
| EP0061408B1 (fr) | 1985-01-16 |
| CA1190936A (en) | 1985-07-23 |
| US4436919A (en) | 1984-03-13 |
| DK132782A (da) | 1982-09-26 |
| NO155441C (no) | 1987-04-01 |
| PL130111B1 (en) | 1984-07-31 |
| ATE11292T1 (de) | 1985-02-15 |
| NO155441B (no) | 1986-12-22 |
| DK158583C (da) | 1990-11-05 |
| NO820963L (no) | 1982-09-27 |
| DE3261902D1 (de) | 1985-02-28 |
| MX7053E (es) | 1987-04-08 |
| FI68240B (fi) | 1985-04-30 |
| KR860000588B1 (ko) | 1986-05-17 |
| AU547100B2 (en) | 1985-10-03 |
| PL235608A1 (en) | 1983-03-14 |
| DK158583B (da) | 1990-06-11 |
| KR830009081A (ko) | 1983-12-17 |
| JPS57206689A (en) | 1982-12-18 |
| AR227966A1 (es) | 1982-12-30 |
| FI820970L (fi) | 1982-09-26 |
| AU8186482A (en) | 1982-09-30 |
| ZA821644B (en) | 1983-01-26 |
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