JPH0148902B2 - - Google Patents
Info
- Publication number
- JPH0148902B2 JPH0148902B2 JP12594181A JP12594181A JPH0148902B2 JP H0148902 B2 JPH0148902 B2 JP H0148902B2 JP 12594181 A JP12594181 A JP 12594181A JP 12594181 A JP12594181 A JP 12594181A JP H0148902 B2 JPH0148902 B2 JP H0148902B2
- Authority
- JP
- Japan
- Prior art keywords
- solvent
- chlorophenyl
- reaction
- deoxidizing agent
- amino
- 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
- 239000002904 solvent Substances 0.000 claims description 13
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 12
- JJWKPURADFRFRB-UHFFFAOYSA-N carbonyl sulfide Chemical compound O=C=S JJWKPURADFRFRB-UHFFFAOYSA-N 0.000 claims description 12
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical group [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- -1 (4-chlorophenyl)-2-thiazolidone Chemical compound 0.000 claims description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 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 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- TYRGSDXYMNTMML-UHFFFAOYSA-N propyl hydrogen sulfate Chemical compound CCCOS(O)(=O)=O TYRGSDXYMNTMML-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Thiazole And Isothizaole Compounds (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12594181A JPS5829777A (ja) | 1981-08-13 | 1981-08-13 | トランス−4−メチル−5−(4−クロロフエニル)−2−チアゾリドンの製造方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12594181A JPS5829777A (ja) | 1981-08-13 | 1981-08-13 | トランス−4−メチル−5−(4−クロロフエニル)−2−チアゾリドンの製造方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5829777A JPS5829777A (ja) | 1983-02-22 |
JPH0148902B2 true JPH0148902B2 (ru) | 1989-10-20 |
Family
ID=14922755
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12594181A Granted JPS5829777A (ja) | 1981-08-13 | 1981-08-13 | トランス−4−メチル−5−(4−クロロフエニル)−2−チアゾリドンの製造方法 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5829777A (ru) |
-
1981
- 1981-08-13 JP JP12594181A patent/JPS5829777A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5829777A (ja) | 1983-02-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS6024781B2 (ja) | シス−2−ヒドロキシ−2−フエニル−r−1−シクロヘキサンカルボン酸の製造法 | |
JPH0148902B2 (ru) | ||
JPS6145613B2 (ru) | ||
JPS629098B2 (ru) | ||
JPH0136818B2 (ru) | ||
JP2526950B2 (ja) | 新規なアルデヒド化合物 | |
JP2716243B2 (ja) | N―ベンジル―3―ヒドロキシスクシンアミド酸およびその製造法 | |
JPH0696564B2 (ja) | α−(ω−ヒドロキシアルキル)フルフリルアルコ−ル及びその製造法 | |
JPH0148900B2 (ru) | ||
JPS6241510B2 (ru) | ||
JPH0251418B2 (ru) | ||
JPS6026395B2 (ja) | N−トリアルキルシリルメチル尿素の合成法 | |
Sera et al. | Photoreaction of N, N'-dibromo-2, 5-piperazinedione. | |
JPH0316337B2 (ru) | ||
JPH0316339B2 (ru) | ||
JPS5951940B2 (ja) | ピペリジノアルカノ−ル類の製造法 | |
JPS62230743A (ja) | 1−アルコキシ−2−メチルナフタレンの製造法 | |
JPS6228782B2 (ru) | ||
JPS6228781B2 (ru) | ||
JPH027583B2 (ru) | ||
JPS5846513B2 (ja) | 2↓−アロイルホルミル置換ピロ−ル誘導体及びその製造方法 | |
JPH07173145A (ja) | 3−フタリジリデン酢酸アルキルエステルの製造方法 | |
JPH0148901B2 (ru) | ||
JPH10182523A (ja) | 1位置換−2,2−ジフロロ−3−ブテン−1−オール類の製造法 | |
JPH03127780A (ja) | アニリノピリミジン誘導体 |