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Ammonium Hydroxide → 5-Chloropentanesulfonamide

HRID 724801
ノート
印刷プレビュー

反応式

HRID 724801 の反応式
[OH-].[NH4+:2].[Cl:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][S:9](Cl)(=[O:11])=[O:10]>O1CCCC1>[Cl:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][S:9]([NH2:2])(=[O:11])=[O:10]
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 14923Ammonium HydroxideHCID 12589202HCID 12589202、化合物

生成物 1

HCID 99899625-Chloropentanesulfonamide

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

2.5 ml of a 28% aqueous solution of ammonium hydroxide were added dropwise at 0° to +5° C. under an inert gas atmosphere to a solution of 2.5 g of 5-chloropentane sulfonyl chloride (preparation described in: Bull. Soc. Chim. Belg. (1965) Vol. 74, p. 21) in 30 ml of tetrahydrofuran. The temperature was allowed to rise from 3° C. to 16° C., and the mixture was stirred at ambient temperature for 2 hours. The tetrahydrofuran was evaporated under reduced pressure and the residue was taken up in water, extracted with methylene chloride, washed with water, then with an aqueous solution of sodium chloride,. dried and evaporated under reduced pressure to obtain 2.01 g of the expected product melting at 62° C.

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

後処理

  1. customto rise from 3° C. to 16° C.
  2. customThe tetrahydrofuran was evaporated under reduced pressure
  3. extractionextracted with methylene chloride
  4. washwashed with water
  5. customdried
  6. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-4cfcf85d2aa046b388163851ec267598
出典データセット
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05705494

反応ノート

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