JPH0318617B2 - - Google Patents
Info
- Publication number
- JPH0318617B2 JPH0318617B2 JP57071292A JP7129282A JPH0318617B2 JP H0318617 B2 JPH0318617 B2 JP H0318617B2 JP 57071292 A JP57071292 A JP 57071292A JP 7129282 A JP7129282 A JP 7129282A JP H0318617 B2 JPH0318617 B2 JP H0318617B2
- Authority
- JP
- Japan
- Prior art keywords
- reaction
- mol
- iodine
- red phosphorus
- solution
- 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 - Lifetime
Links
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 30
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical class SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 claims description 27
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 23
- 239000011630 iodine Substances 0.000 claims description 23
- 229910052740 iodine Inorganic materials 0.000 claims description 23
- 238000004519 manufacturing process Methods 0.000 claims description 18
- 229910000039 hydrogen halide Inorganic materials 0.000 claims description 5
- 239000012433 hydrogen halide Substances 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 239000011574 phosphorus Substances 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 27
- 239000000243 solution Substances 0.000 description 22
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 229910001868 water Inorganic materials 0.000 description 14
- 239000003638 chemical reducing agent Substances 0.000 description 13
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
- CSKNSYBAZOQPLR-UHFFFAOYSA-N benzenesulfonyl chloride Chemical compound ClS(=O)(=O)C1=CC=CC=C1 CSKNSYBAZOQPLR-UHFFFAOYSA-N 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 238000010992 reflux Methods 0.000 description 10
- 239000012044 organic layer Substances 0.000 description 9
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 7
- WLHCBQAPPJAULW-UHFFFAOYSA-N 4-methylbenzenethiol Chemical compound CC1=CC=C(S)C=C1 WLHCBQAPPJAULW-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 5
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 5
- 239000011701 zinc Substances 0.000 description 5
- 229910052725 zinc Inorganic materials 0.000 description 5
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 3
- -1 aromatic mercaptans Chemical class 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- LLMLGZUZTFMXSA-UHFFFAOYSA-N 2,3,4,5,6-pentachlorobenzenethiol Chemical compound SC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LLMLGZUZTFMXSA-UHFFFAOYSA-N 0.000 description 2
- VFFGBIGCMPVQMT-UHFFFAOYSA-N 2,6-dichloro-4-fluorobenzenethiol Chemical compound FC1=CC(Cl)=C(S)C(Cl)=C1 VFFGBIGCMPVQMT-UHFFFAOYSA-N 0.000 description 2
- LXUNZSDDXMPKLP-UHFFFAOYSA-N 2-Methylbenzenethiol Chemical compound CC1=CC=CC=C1S LXUNZSDDXMPKLP-UHFFFAOYSA-N 0.000 description 2
- HDECRAPHCDXMIJ-UHFFFAOYSA-N 2-methylbenzenesulfonyl chloride Chemical compound CC1=CC=CC=C1S(Cl)(=O)=O HDECRAPHCDXMIJ-UHFFFAOYSA-N 0.000 description 2
- ZDEUGINAVLMAET-UHFFFAOYSA-N 3-fluorobenzenethiol Chemical compound FC1=CC=CC(S)=C1 ZDEUGINAVLMAET-UHFFFAOYSA-N 0.000 description 2
- VZXOZSQDJJNBRC-UHFFFAOYSA-N 4-chlorobenzenethiol Chemical compound SC1=CC=C(Cl)C=C1 VZXOZSQDJJNBRC-UHFFFAOYSA-N 0.000 description 2
- WMUBERLZPXKQLZ-UHFFFAOYSA-N 4-fluoro-2,6-dimethylbenzenethiol Chemical compound CC1=CC(F)=CC(C)=C1S WMUBERLZPXKQLZ-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
- 229910000043 hydrogen iodide Inorganic materials 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000001256 steam distillation Methods 0.000 description 2
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- XGHCLHAVHVHBMO-UHFFFAOYSA-N 2,3,4,5,6-pentachlorobenzenesulfonyl chloride Chemical compound ClC1=C(Cl)C(Cl)=C(S(Cl)(=O)=O)C(Cl)=C1Cl XGHCLHAVHVHBMO-UHFFFAOYSA-N 0.000 description 1
- ICHYMVBIIFENJM-UHFFFAOYSA-N 2,6-dichloro-4-fluorobenzenesulfonyl chloride Chemical compound FC1=CC(Cl)=C(S(Cl)(=O)=O)C(Cl)=C1 ICHYMVBIIFENJM-UHFFFAOYSA-N 0.000 description 1
- OKYSUJVCDXZGKE-UHFFFAOYSA-N 3-fluorobenzenesulfonyl chloride Chemical compound FC1=CC=CC(S(Cl)(=O)=O)=C1 OKYSUJVCDXZGKE-UHFFFAOYSA-N 0.000 description 1
- ZLYBFBAHAQEEQQ-UHFFFAOYSA-N 4-chlorobenzenesulfonyl chloride Chemical compound ClC1=CC=C(S(Cl)(=O)=O)C=C1 ZLYBFBAHAQEEQQ-UHFFFAOYSA-N 0.000 description 1
- RVCGNZNOJBRAGG-UHFFFAOYSA-N 4-fluoro-2,6-dimethylbenzenesulfonyl chloride Chemical compound CC1=CC(F)=CC(C)=C1S(Cl)(=O)=O RVCGNZNOJBRAGG-UHFFFAOYSA-N 0.000 description 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 238000001994 activation Methods 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910001516 alkali metal iodide Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000003317 industrial substance Substances 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 229940053653 phosphorus / potassium Drugs 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
- OBSZRRSYVTXPNB-UHFFFAOYSA-N tetraphosphorus Chemical compound P12P3P1P32 OBSZRRSYVTXPNB-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7129282A JPS58188854A (ja) | 1982-04-30 | 1982-04-30 | ベンゼンチオ−ル類の改良製法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP7129282A JPS58188854A (ja) | 1982-04-30 | 1982-04-30 | ベンゼンチオ−ル類の改良製法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58188854A JPS58188854A (ja) | 1983-11-04 |
| JPH0318617B2 true JPH0318617B2 (it) | 1991-03-13 |
Family
ID=13456462
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP7129282A Granted JPS58188854A (ja) | 1982-04-30 | 1982-04-30 | ベンゼンチオ−ル類の改良製法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58188854A (it) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1380572A1 (en) * | 2001-04-17 | 2004-01-14 | Japan Science and Technology Corporation | Polymercaptopolyphenyls and method for synthesis thereof |
| US20090082590A1 (en) * | 2005-05-17 | 2009-03-26 | Sumitomo Seika Chemicals Co., Ltd. | 4-Mercaptophenyl ester of acetic acid and process for producing the same |
-
1982
- 1982-04-30 JP JP7129282A patent/JPS58188854A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58188854A (ja) | 1983-11-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN107922325B (zh) | 制备二芳基砜的改进方法 | |
| JP5930930B2 (ja) | メチレンジスルホニルクロライド化合物、メチレンジスルホン酸化合物およびメチレンジスルホネート化合物の製造方法 | |
| JP4936630B2 (ja) | ２，２’−ジチオビス（エタンスルホン酸）二ナトリウムの調製のためのプロセス | |
| JPS6147831B2 (it) | ||
| JP4407062B2 (ja) | ジフェニルジスルフィド誘導体の製造法 | |
| JPH0135809B2 (it) | ||
| JPH0318617B2 (it) | ||
| EP1150949B1 (en) | Synthesis of mercapto-benzaldehydes | |
| US3136800A (en) | Method for producing hydroxythiobenzoic acids and esters thereof | |
| JPH0623168B2 (ja) | ベンゼンスルホニルクロリド誘導体の製造方法 | |
| JPH027950B2 (it) | ||
| JPH09157191A (ja) | （ｅ）−スチルベン類の製造方法 | |
| JP3174968B2 (ja) | ２−ハロゲノ−６−置換チオベンゾニトリル類の製造法 | |
| JP2001058968A (ja) | １，３−ジ（２−ｐ−ヒドロキシフェニル−２−プロピル）ベンゼンの製造方法 | |
| JP3799580B2 (ja) | Ｎ−置換−ｎ−スルホニルアミド類の製造方法 | |
| JPH0453860B2 (it) | ||
| KR910003635B1 (ko) | 2-(2-나프틸옥시)프로피온아닐리드 유도체의 제조방법 | |
| JPH0710829B2 (ja) | ベンジルメルカプタン誘導体の製造法 | |
| EP0163506B1 (en) | Process for the preparation of a pyridil-propanoic acid | |
| JPH0357890B2 (it) | ||
| JPS63227564A (ja) | アリルスルホンの製造法 | |
| KR860000262B1 (ko) | 발레로 니트릴로부터 디-치환된 니트릴유도체의 제조방법 | |
| JP2521100B2 (ja) | ハロゲノアルキルフルフリルアルコ−ル類およびその製造法 | |
| JPH0278692A (ja) | Ｓ，ｏ−ジアルキル（２−オキソ−３−チアゾリジニル）ホスホノチオレートの製造方法 | |
| JPS6317060B2 (it) |