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Ammonia → A 643C

HRID 1277487
ノート
印刷プレビュー

反応式

HRID 1277487 の反応式
Cl[CH2:2][C:3]([NH:5][C:6]([CH3:13])([CH3:12])[CH2:7][CH2:8][CH2:9][CH2:10][CH3:11])=[O:4].[NH3:14]>O.C(O)C>[NH2:14][CH2:2][C:3]([NH:5][C:6]([CH3:13])([CH3:12])[CH2:7][CH2:8][CH2:9][CH2:10][CH3:11])=[O:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 222AmmoniaHCID 234541292-chloro-N-(1,1-dimethylhexyl)acetamide

生成物 1

HCID 128299A 643C

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

A suspension of 2-Chloro-N-(1,1-dimethylhexyl)acetamide (2.5 g, 12 m mol) in a mixture of water (50 ml) and ethanol (50 ml) was saturated in ammoniain the cold and held at room temperature for two days with the occasional passage of ammonia. The mixture was evaporated to a gum which was partially dried by azeotroping with ethanol then 40-60 petrol. The residuewas dissolved in chloroform (50 ml) and stirred with sodium carbonate (2 g)and water (10 ml) for 1/2 hour. The organic phase was then separated, driedover magnesium sulphate, evaporated to a yellow oil and distilled to give 2-amino-N-(1,1-dimethylhexyl)acetamide as a colourless oil, b.p. 109°-113° C. at 0.4 mm Hg.

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. customThe mixture was evaporated to a gum which
  2. customwas partially dried
  3. customby azeotroping with ethanol
  4. dissolutionThe residuewas dissolved in chloroform (50 ml)
  5. customThe organic phase was then separated, driedover magnesium sulphate
  6. customevaporated to a yellow oil
  7. distillationdistilled

出典と根拠

ORDレコード
ord-5eec591ef2084b67936a31f67b0a447b
出典データセット
uspto-grants-1981_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04277498

反応ノート

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