JPH0512345B2 - - Google Patents
Info
- Publication number
- JPH0512345B2 JPH0512345B2 JP62090140A JP9014087A JPH0512345B2 JP H0512345 B2 JPH0512345 B2 JP H0512345B2 JP 62090140 A JP62090140 A JP 62090140A JP 9014087 A JP9014087 A JP 9014087A JP H0512345 B2 JPH0512345 B2 JP H0512345B2
- Authority
- JP
- Japan
- Prior art keywords
- sulfide
- hydroxyphenyl
- present
- mercaptophenol
- bis
- 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 - Fee Related
Links
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 16
- BLDLRWQLBOJPEB-UHFFFAOYSA-N 2-(2-hydroxyphenyl)sulfanylphenol Chemical compound OC1=CC=CC=C1SC1=CC=CC=C1O BLDLRWQLBOJPEB-UHFFFAOYSA-N 0.000 claims description 15
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 13
- 239000002904 solvent Substances 0.000 claims description 13
- 238000004519 manufacturing process Methods 0.000 claims description 11
- PXJJSXABGXMUSU-UHFFFAOYSA-N disulfur dichloride Chemical compound ClSSCl PXJJSXABGXMUSU-UHFFFAOYSA-N 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 150000005215 alkyl ethers Chemical class 0.000 claims 1
- 239000000178 monomer Substances 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 11
- -1 ethylene glycol monoalkyl ethers Chemical class 0.000 description 9
- BXAVKNRWVKUTLY-UHFFFAOYSA-N 4-sulfanylphenol Chemical compound OC1=CC=C(S)C=C1 BXAVKNRWVKUTLY-UHFFFAOYSA-N 0.000 description 8
- VMKYTRPNOVFCGZ-UHFFFAOYSA-N 2-sulfanylphenol Chemical compound OC1=CC=CC=C1S VMKYTRPNOVFCGZ-UHFFFAOYSA-N 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000006227 byproduct Substances 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 230000002829 reductive effect Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N anhydrous diethylene glycol Natural products OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- NLXGURFLBLRZRO-UHFFFAOYSA-N 1-chloro-2-(2-chloroethoxymethoxy)ethane Chemical compound ClCCOCOCCCl NLXGURFLBLRZRO-UHFFFAOYSA-N 0.000 description 1
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 description 1
- QVCPYLHXFNQALA-UHFFFAOYSA-N 4-[2-(ethoxymethoxy)ethylsulfanyl]phenol Chemical compound CCOCOCCSC1=CC=C(O)C=C1 QVCPYLHXFNQALA-UHFFFAOYSA-N 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62090140A JPS63255260A (ja) | 1987-04-13 | 1987-04-13 | ビス（ヒドロキシフエニル）スルフイドの製造方法 |
| US07/177,620 US4845299A (en) | 1987-04-13 | 1988-04-05 | Method for the preparation of bis(hydroxyphenyl) sulfides |
| DE8888303164T DE3860588D1 (de) | 1987-04-13 | 1988-04-08 | Verfahren zur herstellung eines bis-(hydroxyphenyl)-sulfids. |
| EP88303164A EP0287292B1 (en) | 1987-04-13 | 1988-04-08 | A method for the preparation of a bis(hydroxyphenyl) sulfide |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP62090140A JPS63255260A (ja) | 1987-04-13 | 1987-04-13 | ビス（ヒドロキシフエニル）スルフイドの製造方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63255260A JPS63255260A (ja) | 1988-10-21 |
| JPH0512345B2 true JPH0512345B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1993-02-17 |
Family
ID=13990205
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP62090140A Granted JPS63255260A (ja) | 1987-04-13 | 1987-04-13 | ビス（ヒドロキシフエニル）スルフイドの製造方法 |
Country Status (4)
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2051229A1 (en) * | 1990-09-14 | 1992-03-15 | Sing-Yuen Sit | Hypocholesterolemic unsymmetrical dithiol ketals |
| GB9415624D0 (en) | 1994-08-01 | 1994-09-21 | Exxon Chemical Patents Inc | Preparation of sulfurised phenol additives intermediates and compositions |
| KR20030091463A (ko) * | 2002-05-28 | 2003-12-03 | 주식회사 엠엔비그린어스 | 방향족황화합물의 제조방법 및 그 방법에 의하여 제조되는방향족황화합물 |
| CN101272853A (zh) * | 2005-08-11 | 2008-09-24 | 国际壳牌研究有限公司 | 成型催化剂的制备方法、催化剂和催化剂的用途 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE249699C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | ||||
| US3057926A (en) * | 1958-03-12 | 1962-10-09 | Ethyl Corp | Sulfur-containing phenolic compounds |
| US3060121A (en) * | 1960-04-04 | 1962-10-23 | Ethyl Corp | Antioxidants |
| US3726928A (en) * | 1969-11-24 | 1973-04-10 | Ferro Corp | 2,2{40 -thiobis(4,6-di-tert.-butylresourcinol) |
| JPS61275263A (ja) * | 1985-04-30 | 1986-12-05 | Seitetsu Kagaku Co Ltd | メルカプトフエノ−ル類の製法 |
| JPH0524233A (ja) * | 1991-07-25 | 1993-02-02 | Fuji Photo Film Co Ltd | サーマルヘツド |
-
1987
- 1987-04-13 JP JP62090140A patent/JPS63255260A/ja active Granted
-
1988
- 1988-04-05 US US07/177,620 patent/US4845299A/en not_active Expired - Fee Related
- 1988-04-08 DE DE8888303164T patent/DE3860588D1/de not_active Expired - Fee Related
- 1988-04-08 EP EP88303164A patent/EP0287292B1/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| EP0287292B1 (en) | 1990-09-12 |
| JPS63255260A (ja) | 1988-10-21 |
| EP0287292A1 (en) | 1988-10-19 |
| DE3860588D1 (de) | 1990-10-18 |
| US4845299A (en) | 1989-07-04 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313111 |
|
| R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
| LAPS | Cancellation because of no payment of annual fees |