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Ammonia → 4-amino-N,1-dimethyl-2-oxo-3-pentenesulfonamide

HRID 1252255
ノート
印刷プレビュー

反応式

HRID 1252255 の反応式
[NH3:1].[CH3:2][N:3]1[C:8]([CH3:9])=[CH:7][C:6](=[O:10])[CH:5]([CH3:11])[S:4]1(=[O:13])=[O:12]>CO>[NH2:1][C:8]([CH3:9])=[CH:7][C:6](=[O:10])[CH:5]([CH3:11])[S:4]([NH:3][CH3:2])(=[O:13])=[O:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 222AmmoniaHCID 201410512,3,6-trimethyl-2H-1,2-thiazin-5(6H)-one 1,1-dioxide

生成物 1

HCID 867421514-amino-N,1-dimethyl-2-oxo-3-pentenesulfonamide

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A moderately rapid stream of dry ammonia was introduced at 20°-25° during 3 hours into a solution of 2.5 g of 2,3,6-trimethyl-2H-1,2-thiazin-5(6H)-one 1,1-dioxide in 25 ml of methanol and the mixture was thereupon left to stand overnight. The dark yellow solution obtained was concentrated to dryness under reduced pressure and the crystalline residue was recrystallized from ethanol. There were obtained 2.3 g of 4-amino-N,1-dimethyl-2-oxo-3-pentenesulfonamide in the form of colorless crystals, m.p. 140°-143°.

後処理

  1. waitthe mixture was thereupon left
  2. customThe dark yellow solution obtained
  3. concentrationwas concentrated to dryness under reduced pressure
  4. customthe crystalline residue was recrystallized from ethanol

出典と根拠

ORDレコード
ord-7c664e08997b42b489d60152ce5b2e87
出典データセット
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04742069

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート