2-Methylsulfinyl-4-(4-trifluoromethylphenyl)benzonitrile → 2-Mercapto-4-(4-trifluoromethylphenyl)benzonitrile

HRID 1432757ノート

反応式

HRID 1432757 の反応式
C[S:2]([C:4]1[CH:11]=[C:10]([C:12]2[CH:17]=[CH:16][C:15]([C:18]([F:21])([F:20])[F:19])=[CH:14][CH:13]=2)[CH:9]=[CH:8][C:5]=1[C:6]#[N:7])=O>FC(F)(F)C(OC(=O)C(F)(F)F)=O>[SH:2][C:4]1[CH:11]=[C:10]([C:12]2[CH:17]=[CH:16][C:15]([C:18]([F:19])([F:20])[F:21])=[CH:14][CH:13]=2)[CH:9]=[CH:8][C:5]=1[C:6]#[N:7]

参加物

3

反応物 1

HCID 221709512-Methylsulfinyl-4-(4-trifluoromethylphenyl)benzonitrile2 回

生成物 1

HCID 121376372-Mercapto-4-(4-trifluoromethylphenyl)benzonitrile収率 51%

試薬・触媒・溶媒 1

HCID 9845Trifluoroacetic anhydride溶媒

実験手順

2.2 g (7.1 mmol) of 2-methylsulfinyl-4-(4-trifluoromethylphenyl)benzonitrile prepared in (b) was stirred in 15 ml of trifluoroacetic anhydride at room temperature for 12 hours, and the low-boiling matters were distilled off under reduced pressure. 50 ml of methanol and 3 g of 20% aqueous potassium hydroxide were added to the residue, and the reaction was carried out for 1 hour. The solvent was distilled off under reduced pressure, and the residue was mixed with 5% aqueous sulfuric acid and extracted with ethyl acetate. The ethyl acetate layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to obtain 1.0 g of 2-mercapto-4-(4-trifluoromethylphenyl)benzonitrile (yield 51.0%), which was used in Example 1 as the starting material.

後処理

  1. distillationthe low-boiling matters were distilled off under reduced pressure
  2. addition50 ml of methanol and 3 g of 20% aqueous potassium hydroxide were added to the residue
  3. distillationThe solvent was distilled off under reduced pressure
  4. additionthe residue was mixed with 5% aqueous sulfuric acid
  5. extractionextracted with ethyl acetate
  6. dry with materialThe ethyl acetate layer was dried over anhydrous sodium sulfate
  7. distillationthe solvent was distilled off under reduced pressure

出典と根拠

ORDレコード
ord-ad186fe202ff4741ae3ffdd116700b78
出典データセット
uspto-grants-2009_11
特許番号
US07612105B2

反応ノート

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