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Methanol → alpha-(2-Benzothiazolylthio)(m-benzoylphenyl)-acetonitrile

HRID 1759437
ノート
印刷プレビュー

反応式

HRID 1759437 の反応式
CO.C1(C)C=CC(S(O[CH:13]([C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([C:22](=[O:29])[C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[CH:17]=2)[C:14]#[N:15])(=O)=O)=CC=1.[Na].[SH:32][C:33]1[S:34][C:35]2[CH:41]=[CH:40][CH:39]=[CH:38][C:36]=2[N:37]=1>O.COCCOC>[S:34]1[C:35]2[CH:41]=[CH:40][CH:39]=[CH:38][C:36]=2[N:37]=[C:33]1[S:32][CH:13]([C:16]1[CH:21]=[CH:20][CH:19]=[C:18]([C:22](=[O:29])[C:23]2[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=2)[CH:17]=1)[C:14]#[N:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 887MethanolHCID 5360545SodiumHCID 12945137O-(p-toluenesulfonyl)-m-benzoylmandelonitrileHCID 178418395HCID 178418395、化合物

生成物 1

HCID 20532028alpha-(2-Benzothiazolylthio)(m-benzoylphenyl)-acetonitrile収率 83.4%

試薬・触媒・溶媒 2

HCID 962Water
溶媒
HCID 80711,2-Dimethoxyethane溶媒

実験手順

Methanol (6 ml) and 3 ml of DME were added to 1.18 g of O-(p-toluenesulfonyl)-m-benzoylmandelonitrile, and the mixture was stirred in an argon atmosphere under ice cooling. Sodium salt of 2-mercaptobenzothiazole (570 mg) was added, and the mixture was stirred for 1.5 hours under ice cooling. Water (50 ml) was added, and the mixture was extracted with 30 ml of methylene chloride three times. The extract was washed with 40 ml of water, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was separated by column chromatography (silica gel; methylene chloride) to afford 972 mg (yield 83%) of alpha-(2-benzothiazolylthio)-(m-benzoylphenyl)acetonitrile as a pale yellow oil.

後処理

  1. stirringthe mixture was stirred for 1.5 hours under ice cooling
  2. extractionthe mixture was extracted with 30 ml of methylene chloride three times
  3. washThe extract was washed with 40 ml of water
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was separated by column chromatography (silica gel; methylene chloride)

出典と根拠

ORDレコード
ord-0a9a5c045719438984471800f79025f1
出典データセット
uspto-grants-1982_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04340740

反応ノート

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