KR900004661A - 3-아릴이소부틸알코올의 제조방법 - Google Patents
3-아릴이소부틸알코올의 제조방법 Download PDFInfo
- Publication number
- KR900004661A KR900004661A KR1019890012715A KR890012715A KR900004661A KR 900004661 A KR900004661 A KR 900004661A KR 1019890012715 A KR1019890012715 A KR 1019890012715A KR 890012715 A KR890012715 A KR 890012715A KR 900004661 A KR900004661 A KR 900004661A
- Authority
- KR
- South Korea
- Prior art keywords
- arylcarbinol
- propanol
- formula
- reacted
- reaction
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 7
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N iso-butyl alcohol Natural products CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 title claims 2
- 229940035429 isobutyl alcohol Drugs 0.000 title claims 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims 12
- 238000006243 chemical reaction Methods 0.000 claims 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims 1
- 150000001340 alkali metals Chemical class 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 230000003197 catalytic effect Effects 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 238000006356 dehydrogenation reaction Methods 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/32—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions without formation of -OH groups
- C07C29/34—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions without formation of -OH groups by condensation involving hydroxy groups or the mineral ester groups derived therefrom, e.g. Guerbet reaction
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C33/00—Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C33/18—Monohydroxylic alcohols containing only six-membered aromatic rings as cyclic part
- C07C33/20—Monohydroxylic alcohols containing only six-membered aromatic rings as cyclic part monocyclic
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (6)
- 밀폐된 반응용기내에서 250 내지 350℃로 수산화알칼리금속 또는 알칼리금속 알코올레이트의 촉매적양의 존재하에 다음식(Ⅱ)의 아릴카르비놀과 n-프로판올을 반응시킴을 특징으로 하는 다음식(I)의 3-아릴이소부틸알코올의 제조방법:상기식에서, R1및 R2는 각각 수소 또는 C8이하의 알킬 또는 시클로알킬기이다.상기식에서, R1및 R2는 상기에 정의한 바와같다.
- 제1항에 있어서, 식(Ⅱ)의 아릴카르비놀은 반응혼합물에 대해 0.5 내지 2중량%의 NaOH 또는 NOH의 존재하에 n-프로판올과 반응함을 특징으로 하는 방법.
- 제1항에 있어서, 식(Ⅱ)의 아릴카르비놀은 약 1:1의 몰비로 n-프로판올과 반응함을 특징으로 하는 방법.
- 제1항에 있어서, 식(Ⅱ)의 아릴카르비놀이 n-프로판올과 반응함을 특징으로 하는 방법.상기식에서, R1이 메틸, 이소프로필 또는 3차-부틸이고, R2는 수소이다.
- 제1항에 있어서, 식(Ⅱ)의 아릴카르비놀이 탈수소 촉매의 부재하에 n-프로판올과 반응함을 특징으로 하는 방법.
- 제1항에 있어서, 반응동안에 형성된 반응수가 식(Ⅱ)의 아릴카르비놀과 n-프로판올과 반응중에 증류제거되지 않음을 특징으로 하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3830019A DE3830019A1 (de) | 1988-09-03 | 1988-09-03 | Verfahren zur herstellung von 3-aryl-isobutylalkoholen |
DEP3830019.2 | 1988-09-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR900004661A true KR900004661A (ko) | 1990-04-12 |
Family
ID=6362253
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019890012715A KR900004661A (ko) | 1988-09-03 | 1989-09-02 | 3-아릴이소부틸알코올의 제조방법 |
Country Status (7)
Country | Link |
---|---|
US (1) | US4987270A (ko) |
EP (1) | EP0358088B1 (ko) |
JP (1) | JPH02115137A (ko) |
KR (1) | KR900004661A (ko) |
DE (2) | DE3830019A1 (ko) |
ES (1) | ES2055768T3 (ko) |
HU (1) | HU203713B (ko) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4447361A1 (de) * | 1994-12-21 | 1996-06-27 | Schuelke & Mayr Gmbh | Biozide Alkohole, ihre Herstellung und ihre Verwendung |
JP5854345B2 (ja) * | 2010-03-05 | 2016-02-09 | 国立大学法人名古屋大学 | 二量体の製造方法 |
BR102019024934B1 (pt) | 2019-11-26 | 2022-02-22 | Petróleo Brasileiro S.A. - Petrobras | Processo para obtenção de compostos, dentre os quais o triptano por reação de acoplamento de álcoois |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2457866A (en) * | 1945-05-26 | 1949-01-04 | Carbide & Carbon Chem Corp | Condensation of alcohols |
US2645667A (en) * | 1951-10-01 | 1953-07-14 | Phillips Petroleum Co | Condensation of alcohols in the presence of calcium hydroxide |
US3119880A (en) * | 1961-05-29 | 1964-01-28 | Gulf Research Development Co | Condensation of alcohols |
US3328470A (en) * | 1963-10-03 | 1967-06-27 | Continental Oil Co | Greater selectivity in the guerbet reaction |
NL6706692A (ko) * | 1966-05-18 | 1967-11-20 | ||
NL6709801A (ko) * | 1966-07-21 | 1968-01-22 | ||
DE2124589C3 (de) * | 1971-05-18 | 1975-06-05 | Basf Ag, 6700 Ludwigshafen | Anthrapyrimidin-Farbstoffe und Verfahren zu ihrer Herstellung |
US3860664A (en) * | 1973-06-06 | 1975-01-14 | Continental Oil Co | Process for condensation of alcohols |
DE3520185A1 (de) * | 1985-06-05 | 1986-12-11 | Henkel KGaA, 4000 Düsseldorf | 2-benzylalkanol-1-polyglykolether sowie verfahren zu ihrer herstellung |
DE3546016A1 (de) * | 1985-12-24 | 1987-06-25 | Basf Ag | Verfahren zur herstellung von in 1-stellung durch aromatische oder heterocyclische reste substituierten alkanolen |
DE3712873A1 (de) * | 1987-04-15 | 1988-11-03 | Consortium Elektrochem Ind | 2-methyl- oder 2-methoxyphenylgruppen enthaltende alkohole und deren verwendung als duftstoffe |
-
1988
- 1988-09-03 DE DE3830019A patent/DE3830019A1/de not_active Withdrawn
-
1989
- 1989-08-23 US US07/397,883 patent/US4987270A/en not_active Expired - Fee Related
- 1989-08-29 DE DE8989115892T patent/DE58904784D1/de not_active Expired - Lifetime
- 1989-08-29 EP EP89115892A patent/EP0358088B1/de not_active Expired - Lifetime
- 1989-08-29 ES ES89115892T patent/ES2055768T3/es not_active Expired - Lifetime
- 1989-09-01 HU HU894547A patent/HU203713B/hu not_active IP Right Cessation
- 1989-09-01 JP JP1224761A patent/JPH02115137A/ja active Pending
- 1989-09-02 KR KR1019890012715A patent/KR900004661A/ko not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
HU203713B (en) | 1991-09-30 |
EP0358088B1 (de) | 1993-06-23 |
HUT51588A (en) | 1990-05-28 |
ES2055768T3 (es) | 1994-09-01 |
JPH02115137A (ja) | 1990-04-27 |
DE58904784D1 (de) | 1993-07-29 |
US4987270A (en) | 1991-01-22 |
EP0358088A3 (en) | 1990-05-23 |
EP0358088A2 (de) | 1990-03-14 |
DE3830019A1 (de) | 1990-03-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |