GB980272A - Production of carbinols - Google Patents
Production of carbinolsInfo
- Publication number
- GB980272A GB980272A GB309/63A GB30963A GB980272A GB 980272 A GB980272 A GB 980272A GB 309/63 A GB309/63 A GB 309/63A GB 30963 A GB30963 A GB 30963A GB 980272 A GB980272 A GB 980272A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydroxide
- r1r2r3
- hydroxyisopropyl
- diisopropylbenzene
- cumene
- 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
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 5
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract 3
- 239000012074 organic phase Substances 0.000 abstract 2
- 230000003647 oxidation Effects 0.000 abstract 2
- 238000007254 oxidation reaction Methods 0.000 abstract 2
- VUMCUSHVMYIRMB-UHFFFAOYSA-N 1,3,5-tri(propan-2-yl)benzene Chemical compound CC(C)C1=CC(C(C)C)=CC(C(C)C)=C1 VUMCUSHVMYIRMB-UHFFFAOYSA-N 0.000 abstract 1
- UNEATYXSUBPPKP-UHFFFAOYSA-N 1,3-Diisopropylbenzene Chemical compound CC(C)C1=CC=CC(C(C)C)=C1 UNEATYXSUBPPKP-UHFFFAOYSA-N 0.000 abstract 1
- SPPWGCYEYAMHDT-UHFFFAOYSA-N 1,4-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=C(C(C)C)C=C1 SPPWGCYEYAMHDT-UHFFFAOYSA-N 0.000 abstract 1
- XZISOEPNTDOUEA-UHFFFAOYSA-N 1-fluoro-4-propan-2-ylbenzene Chemical compound CC(C)C1=CC=C(F)C=C1 XZISOEPNTDOUEA-UHFFFAOYSA-N 0.000 abstract 1
- JWCFSPUNILJEOV-UHFFFAOYSA-N 2,4-ditert-butyl-6-methylbenzene-1,3,5-triol Chemical compound CC(C=1C(=C(C(=C(C1O)C)O)C(C)(C)C)O)(C)C JWCFSPUNILJEOV-UHFFFAOYSA-N 0.000 abstract 1
- PSYUWKPFWPMEAY-UHFFFAOYSA-N 2-[3,5-di(propan-2-yl)phenyl]propan-2-ol Chemical compound CC(C)C1=CC(C(C)C)=CC(C(C)(C)O)=C1 PSYUWKPFWPMEAY-UHFFFAOYSA-N 0.000 abstract 1
- BDCFWIDZNLCTMF-UHFFFAOYSA-N 2-phenylpropan-2-ol Chemical compound CC(C)(O)C1=CC=CC=C1 BDCFWIDZNLCTMF-UHFFFAOYSA-N 0.000 abstract 1
- -1 Aralkyl tertiary alcohols Chemical class 0.000 abstract 1
- 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 abstract 1
- 239000004793 Polystyrene Substances 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 150000001717 carbocyclic compounds Chemical group 0.000 abstract 1
- 125000002837 carbocyclic group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- IGARGHRYKHJQSM-UHFFFAOYSA-N cyclohexylbenzene Chemical compound C1CCCCC1C1=CC=CC=C1 IGARGHRYKHJQSM-UHFFFAOYSA-N 0.000 abstract 1
- 229930007927 cymene Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 1
- 239000007791 liquid phase Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 abstract 1
- 229920002223 polystyrene Polymers 0.000 abstract 1
- 229940083608 sodium hydroxide Drugs 0.000 abstract 1
- 235000011121 sodium hydroxide Nutrition 0.000 abstract 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
- C07C29/48—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxidation reactions with formation of hydroxy groups
- C07C29/50—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxidation reactions with formation of hydroxy groups with molecular oxygen only
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16596062A | 1962-01-12 | 1962-01-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB980272A true GB980272A (en) | 1965-01-13 |
Family
ID=22601205
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB309/63A Expired GB980272A (en) | 1962-01-12 | 1963-01-29 | Production of carbinols |
Country Status (2)
| Country | Link |
|---|---|
| GB (1) | GB980272A (ja) |
| LU (1) | LU42994A1 (ja) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3382286A (en) * | 1965-01-21 | 1968-05-07 | Allied Chem | Preparation of aromatic tertiary alcohols by oxidation |
| EP0267759A2 (en) * | 1986-11-07 | 1988-05-18 | Kureha Kagaku Kogyo Kabushiki Kaisha | Oxidation process of aromatic compounds |
| US4746757A (en) * | 1985-07-19 | 1988-05-24 | Kureha Kagaku Kogyo Kabushiki Kaisha | Process for producing (2-hydroxy-2-propyl)-naphthalene compounds |
-
1963
- 1963-01-10 LU LU42994D patent/LU42994A1/xx unknown
- 1963-01-29 GB GB309/63A patent/GB980272A/en not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3382286A (en) * | 1965-01-21 | 1968-05-07 | Allied Chem | Preparation of aromatic tertiary alcohols by oxidation |
| US4746757A (en) * | 1985-07-19 | 1988-05-24 | Kureha Kagaku Kogyo Kabushiki Kaisha | Process for producing (2-hydroxy-2-propyl)-naphthalene compounds |
| EP0267759A2 (en) * | 1986-11-07 | 1988-05-18 | Kureha Kagaku Kogyo Kabushiki Kaisha | Oxidation process of aromatic compounds |
| EP0267759A3 (en) * | 1986-11-07 | 1989-06-14 | Kureha Kagaku Kogyo Kabushiki Kaisha | Oxidation process of aromatic compounds |
Also Published As
| Publication number | Publication date |
|---|---|
| LU42994A1 (ja) | 1963-03-11 |
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