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Formic Acid → 2-Methylaminocarbonylthioethylamine (formate)

HRID 1607103
ノート
印刷プレビュー

反応式

HRID 1607103 の反応式
C1(C(C2C=CC=CC=2)(C2C=CC=CC=2)[NH:8][CH2:9][CH2:10][S:11][C:12]([NH:14][CH3:15])=[O:13])C=CC=CC=1.[CH:28]([OH:30])=[O:29]>>[CH:28]([OH:30])=[O:29].[CH3:15][NH:14][C:12]([S:11][CH2:10][CH2:9][NH2:8])=[O:13]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 284Formic AcidHCID 15616514N-triphenylmethyl-2-methylaminocarbonylthioethylamine

生成物 1

HCID 156165162-Methylaminocarbonylthioethylamine (formate)収率 95%

反応条件

温度
50 °C

実験手順

To N-triphenylmethyl-2-methylaminocarbonylthioethylamine (306 mg) which was prepared by the method of Reference 2 was added formic acid (98%; 5 ml). The reaction solution was stirred at a temperature of 50° C. for 30 minutes and was then concentrated under reduced pressure. The resultant residue was purified without after-treatment by silica gel chromatography using a solvent system of chloroform/methanol/water (6:5:1 v/v) to obtain 139 mg of the desired product with a yield of 95%.

後処理

  1. concentrationwas then concentrated under reduced pressure
  2. customThe resultant residue was purified without after-treatment by silica gel chromatography

出典と根拠

ORDレコード
ord-1659411165b0411b8063ca1665ed9be6
出典データセット
uspto-grants-1989_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04863935

反応ノート

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