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Hydrochloric Acid → N-{3-[(1-Chloro-2-nitroethenyl)sulfanyl]propyl}acetamide

HRID 364860
ノート
印刷プレビュー

反応式

HRID 364860 の反応式
[OH-].[Na+].[SH:3][CH2:4][CH2:5][CH2:6][NH:7][C:8](=[O:10])[CH3:9].[Cl:11][C:12](Cl)=[CH:13][N+:14]([O-:16])=[O:15].Cl.[Cl-].[Na+]>CO>[Cl:11][C:12]([S:3][CH2:4][CH2:5][CH2:6][NH:7][C:8](=[O:10])[CH3:9])=[CH:13][N+:14]([O-:16])=[O: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 5

HCID 313Hydrochloric AcidHCID 5234Sodium ChlorideHCID 14798Sodium HydroxideHCID 122195711,1-Dichloro-2-nitroetheneHCID 20238484N-(3-Mercaptopropyl)acetamide

生成物 1

HCID 53674132N-{3-[(1-Chloro-2-nitroethenyl)sulfanyl]propyl}acetamide

試薬・触媒・溶媒 1

実験手順

A solution of 0.12 g of sodium hydroxide in 5 ml of methanol was added over 10 minutes to a solution of 0.40 g of 1 in 5 ml of methanol. Then a solution of 0.95 g of 1,1-dichloro-2-nitroethene (13A) in 5 ml of methanol was added over 20 minutes, at 0° C. The mixture then was stirred for 20 minutes and poured into 2% hydrochloric acid saturated with sodium chloride. The resulting mixture was extracted with methylene chloride, the solvent was evaporated and the residue was purified over silica gel to give 13, as an oil.

後処理

  1. extractionThe resulting mixture was extracted with methylene chloride
  2. customthe solvent was evaporated
  3. customthe residue was purified over silica gel

出典と根拠

ORDレコード
ord-6598e63fb500430c875ca39206849c0b
出典データセット
uspto-grants-1986_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04606862

反応ノート

読み込み中…

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
HCID 887
Methanol
溶媒
3 回