m-Chloroperbenzoic acid → HCID 23470801、化合物

HRID 127934ノート

反応式

HRID 127934 の反応式
[C:1]([NH:4][C:5]1[CH:10]=[CH:9][C:8]([S:11][CH2:12][CH2:13][CH2:14][Cl:15])=[CH:7][CH:6]=1)(=[O:3])[CH3:2].ClC1C=CC=C(C(OO)=[O:24])C=1>C(Cl)Cl>[C:1]([NH:4][C:5]1[CH:10]=[CH:9][C:8]([S:11]([CH2:12][CH2:13][CH2:14][Cl:15])=[O:24])=[CH:7][CH:6]=1)(=[O:3])[CH3:2]

参加物

4

反応物 2

HCID 70297m-Chloroperbenzoic acidHCID 14005891N-{4-[(3-Chloropropyl)sulfanyl]phenyl}acetamide

生成物 1

HCID 23470801HCID 23470801、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A solution of 1.22 g. (0.005 mole) of 3-(p-acetamidophenylthio)propyl chloride in 25 ml. of methylene chloride is cooled in an ice bath while 0.88 g. (0.005 mole) of m-chloro-perbenzoic acid is added in portions. After keeping at room temperature overnight the reaction mixture is washed with excess 0.5 N sodium hydroxide, dried, and concentrated to a light brown oil. By triturating with ether, 1.06 g. of 3-(p-acetamidophenylsulfinyl)propyl chloride is obtained. Anal. Calcd for C11H14ClNO2S: C, 50.86; H, 5.43; N, 5.39; Cl, 13.65. Found: C, 50.53; H, 5.59; N, 5.23; Cl, 13.67.

後処理

  1. washthe reaction mixture is washed with excess 0.5 N sodium hydroxide
  2. customdried
  3. concentrationconcentrated to a light brown oil
  4. customBy triturating with ether, 1.06 g

出典と根拠

ORDレコード
ord-353255593c3c42538729104a5bc1a34d
出典データセット
uspto-grants-1981_03
特許番号
US04258045

反応ノート

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