GB1332080A - Alkylation process - Google Patents
Alkylation processInfo
- Publication number
- GB1332080A GB1332080A GB3431271A GB3431271A GB1332080A GB 1332080 A GB1332080 A GB 1332080A GB 3431271 A GB3431271 A GB 3431271A GB 3431271 A GB3431271 A GB 3431271A GB 1332080 A GB1332080 A GB 1332080A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phenylphenol
- oxide
- molybdenum
- acid
- alkylation
- 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
- 238000005804 alkylation reaction Methods 0.000 title abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- 239000003054 catalyst Substances 0.000 abstract 3
- 230000029936 alkylation Effects 0.000 abstract 2
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 abstract 2
- 239000000395 magnesium oxide Substances 0.000 abstract 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 abstract 2
- 229910000476 molybdenum oxide Inorganic materials 0.000 abstract 2
- JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 abstract 2
- VLAPMBHFAWRUQP-UHFFFAOYSA-L molybdic acid Chemical compound O[Mo](O)(=O)=O VLAPMBHFAWRUQP-UHFFFAOYSA-L 0.000 abstract 2
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 abstract 2
- 150000002989 phenols Chemical class 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- PXSSNPBEHHJLDH-UHFFFAOYSA-N 2,3,4,5-tetramethylphenol Chemical compound CC1=CC(O)=C(C)C(C)=C1C PXSSNPBEHHJLDH-UHFFFAOYSA-N 0.000 abstract 1
- XRUGBBIQLIVCSI-UHFFFAOYSA-N 2,3,4-trimethylphenol Chemical class CC1=CC=C(O)C(C)=C1C XRUGBBIQLIVCSI-UHFFFAOYSA-N 0.000 abstract 1
- XXKHDSGLCLCFSC-UHFFFAOYSA-N 2,3-diphenylphenol Chemical compound C=1C=CC=CC=1C=1C(O)=CC=CC=1C1=CC=CC=C1 XXKHDSGLCLCFSC-UHFFFAOYSA-N 0.000 abstract 1
- MKRGRCLYQUZXFS-UHFFFAOYSA-N 2,4-diphenylphenol Chemical compound OC1=CC=C(C=2C=CC=CC=2)C=C1C1=CC=CC=C1 MKRGRCLYQUZXFS-UHFFFAOYSA-N 0.000 abstract 1
- CJNVCRCOJLJTIH-UHFFFAOYSA-N 2-(1,2-dimethylcyclohexa-2,4-dien-1-yl)phenol Chemical compound CC1=CC=CCC1(C)C1=CC=CC=C1O CJNVCRCOJLJTIH-UHFFFAOYSA-N 0.000 abstract 1
- NZRROOFTLDWJRD-UHFFFAOYSA-N 2-(2,3,5,6-tetramethylphenyl)phenol Chemical compound CC1=CC(C)=C(C)C(C=2C(=CC=CC=2)O)=C1C NZRROOFTLDWJRD-UHFFFAOYSA-N 0.000 abstract 1
- HINVZCMPYKPBIL-UHFFFAOYSA-N 2-(2,4,6-trimethylphenyl)phenol Chemical compound CC1=CC(C)=CC(C)=C1C1=CC=CC=C1O HINVZCMPYKPBIL-UHFFFAOYSA-N 0.000 abstract 1
- QUVSSVUYCDSKME-UHFFFAOYSA-N 2-(2-methylphenyl)-4-phenylphenol Chemical compound CC1=CC=CC=C1C1=CC(C=2C=CC=CC=2)=CC=C1O QUVSSVUYCDSKME-UHFFFAOYSA-N 0.000 abstract 1
- APNFMEVVIUSJSX-UHFFFAOYSA-N 2-(2-methylphenyl)phenol Chemical compound CC1=CC=CC=C1C1=CC=CC=C1O APNFMEVVIUSJSX-UHFFFAOYSA-N 0.000 abstract 1
- XPZPDODUKIUELL-UHFFFAOYSA-N 2-(4-methyl-3-phenylphenyl)phenol Chemical compound CC1=CC=C(C=2C(=CC=CC=2)O)C=C1C1=CC=CC=C1 XPZPDODUKIUELL-UHFFFAOYSA-N 0.000 abstract 1
- BRDBTVDUEPOHFO-UHFFFAOYSA-N 3-methyl-5-phenylphenol Chemical compound CC1=CC(O)=CC(C=2C=CC=CC=2)=C1 BRDBTVDUEPOHFO-UHFFFAOYSA-N 0.000 abstract 1
- VMMOWSARKBKLJM-UHFFFAOYSA-N 4-methyl-2-phenylphenol Chemical compound CC1=CC=C(O)C(C=2C=CC=CC=2)=C1 VMMOWSARKBKLJM-UHFFFAOYSA-N 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 150000001896 cresols Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 239000005078 molybdenum compound Substances 0.000 abstract 1
- 150000002752 molybdenum compounds Chemical class 0.000 abstract 1
- FXADMRZICBQPQY-UHFFFAOYSA-N orthotelluric acid Chemical compound O[Te](O)(O)(O)(O)O FXADMRZICBQPQY-UHFFFAOYSA-N 0.000 abstract 1
- 229910052714 tellurium Inorganic materials 0.000 abstract 1
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 abstract 1
- LAJZODKXOMJMPK-UHFFFAOYSA-N tellurium dioxide Chemical compound O=[Te]=O LAJZODKXOMJMPK-UHFFFAOYSA-N 0.000 abstract 1
- SITVSCPRJNYAGV-UHFFFAOYSA-N tellurous acid Chemical compound O[Te](O)=O SITVSCPRJNYAGV-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
- 150000003739 xylenols Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/11—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms
- C07C37/16—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by reactions increasing the number of carbon atoms by condensation involving hydroxy groups of phenols or alcohols or the ether or mineral ester group derived therefrom
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)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US5733570A | 1970-07-22 | 1970-07-22 | |
| US5735470A | 1970-07-22 | 1970-07-22 | |
| US5735770A | 1970-07-22 | 1970-07-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1332080A true GB1332080A (en) | 1973-10-03 |
Family
ID=27369231
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3431271A Expired GB1332080A (en) | 1970-07-22 | 1971-07-21 | Alkylation process |
Country Status (5)
| Country | Link |
|---|---|
| JP (1) | JPS5811412B1 (enrdf_load_stackoverflow) |
| DE (3) | DE2167199C2 (enrdf_load_stackoverflow) |
| FR (1) | FR2103233A5 (enrdf_load_stackoverflow) |
| GB (1) | GB1332080A (enrdf_load_stackoverflow) |
| NL (1) | NL7110147A (enrdf_load_stackoverflow) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN117085705A (zh) * | 2022-05-12 | 2023-11-21 | 浙江医药股份有限公司新昌制药厂 | 用于合成邻甲基苯酚的催化剂及其制备方法和利用其合成邻甲基苯酚的方法 |
| CN118063304A (zh) * | 2024-03-11 | 2024-05-24 | 安徽兴隆化工有限公司 | 一种2甲4氯丙酸的制备方法 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6447311U (enrdf_load_stackoverflow) * | 1987-09-14 | 1989-03-23 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3446856A (en) * | 1964-05-29 | 1969-05-27 | Gen Electric | Methylation of phenols |
| US3857899A (en) * | 1968-10-05 | 1974-12-31 | Sumitomo Chemical Co | Process for selective methylation of phenols |
| GB1262177A (en) * | 1968-10-28 | 1972-02-02 | Arakawa Rinsan Kagaku Kogyo | Improvements in and relating to the production of 2,6-xylenol |
-
1971
- 1971-07-21 GB GB3431271A patent/GB1332080A/en not_active Expired
- 1971-07-22 FR FR7126895A patent/FR2103233A5/fr not_active Expired
- 1971-07-22 NL NL7110147A patent/NL7110147A/xx not_active Application Discontinuation
- 1971-07-22 DE DE19712167199 patent/DE2167199C2/de not_active Expired
- 1971-07-22 JP JP46054901A patent/JPS5811412B1/ja active Granted
- 1971-07-22 DE DE19712167290 patent/DE2167290C1/de not_active Expired
- 1971-07-22 DE DE19712136602 patent/DE2136602C3/de not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN117085705A (zh) * | 2022-05-12 | 2023-11-21 | 浙江医药股份有限公司新昌制药厂 | 用于合成邻甲基苯酚的催化剂及其制备方法和利用其合成邻甲基苯酚的方法 |
| CN118063304A (zh) * | 2024-03-11 | 2024-05-24 | 安徽兴隆化工有限公司 | 一种2甲4氯丙酸的制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| DE2136602B2 (de) | 1980-11-27 |
| DE2167199C2 (de) | 1982-01-21 |
| JPS5811412B1 (enrdf_load_stackoverflow) | 1983-03-02 |
| DE2167290C1 (de) | 1982-07-08 |
| NL7110147A (enrdf_load_stackoverflow) | 1972-01-25 |
| DE2136602C3 (de) | 1981-09-17 |
| DE2136602A1 (de) | 1972-02-03 |
| FR2103233A5 (enrdf_load_stackoverflow) | 1972-04-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MX165355B (es) | Mejoras en procedimiento de descomposicion de un producto | |
| JPS6029371B2 (ja) | ヒドロキシベンズアルデヒドの製法 | |
| GB1494350A (en) | Alkylthio phenolic antioxidants | |
| GB1262177A (en) | Improvements in and relating to the production of 2,6-xylenol | |
| GB1332080A (en) | Alkylation process | |
| GB1381398A (en) | Purification and recovery of phenols | |
| US4269735A (en) | Magnesium oxide catalyst | |
| GB2136798A (en) | Preparation of meta-isopropylphenol | |
| US4322566A (en) | Magnesium oxide catalyst | |
| GB1239761A (enrdf_load_stackoverflow) | ||
| GB1461006A (en) | Process for converting alkylaromatic hydroperoxides into phenolic products and carbonyl products | |
| GB754872A (en) | Improvements in or relating to the preparation of a mixture of cymene isomers rich in m- and p-cymene | |
| US2295608A (en) | Alkylation catalyst | |
| GB1228549A (enrdf_load_stackoverflow) | ||
| US2551628A (en) | Isomerization of phenols | |
| DE3278398D1 (en) | Catalyst composition for the ortho-alkylation of a phenol | |
| US4453024A (en) | Process for the meta-hydroxylation of alkylphenols and the ethers thereof in a superacidic medium | |
| Hawkins et al. | A kinetic study of the aminolysis and hydrolysis of α-naphthyl acetate | |
| GB1327365A (en) | Process for preparing catechol and hydroquinone | |
| GB1491529A (en) | Oxidation catalyst | |
| GB1111751A (en) | Process for the arylalkylation of phenols | |
| GB1115116A (en) | Improvements in the production of unsaturated aliphatic monocarboxylic acids | |
| GB1230024A (enrdf_load_stackoverflow) | ||
| GB1384110A (en) | Preparation of 2,6-naphthalene dicarboxylic acid | |
| GB980283A (en) | Process for preparing very pure formaldehyde |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |