Water → Ethyl N-allyl-N-(1-oxoprop-2-yl)-carbamate

HRID 1460766

反応式

HRID 1460766 の反応式
[CH2:1]([N:4]([CH:10]([CH3:16])[CH:11](OC)[O:12]C)[C:5](=[O:9])[O:6][CH2:7][CH3:8])[CH:2]=[CH2:3].O.[Cl-].[Na+]>C(O)=O>[CH2:1]([N:4]([CH:10]([CH3:16])[CH:11]=[O:12])[C:5](=[O:9])[O:6][CH2:7][CH3:8])[CH:2]=[CH2:3]

参加物

5

反応物 3

HCID 962WaterHCID 5234Sodium ChlorideHCID 15069988N-Allyl-N-(1,1-dimethoxyprop-2-yl)-urethane

生成物 1

HCID 15069993Ethyl N-allyl-N-(1-oxoprop-2-yl)-carbamate

試薬・触媒・溶媒 1

HCID 284Formic Acid溶媒

実験手順

182 g (0.7S7 mol) of ethyl N-allyl-N-(1,1-dimethoxyprop -2-yl)-carbamate in 1.5 1 of water are heated under reflux for three hours with 80 ml of formic acid. The mixture is saturated with sodium chloride, the organic phase is separated off and the aqueous phase is extracted twice with 500 ml of methylene chloride each time. The organic solutions are washed with saturated sodium hydrogen carbonate solution until neutral, dried over magnesium sulphate and concentrated, and the residue is distilled.

後処理

  1. customthe organic phase is separated off
  2. extractionthe aqueous phase is extracted twice with 500 ml of methylene chloride each time
  3. washThe organic solutions are washed with saturated sodium hydrogen carbonate solution until neutral,
  4. dry with materialdried over magnesium sulphate
  5. concentrationconcentrated
  6. distillationthe residue is distilled

出典と根拠

ORDレコード
ord-4a56c24f8bbe4384bb23cced35cc2c6b
出典データセット
uspto-grants-1991_12
特許番号
US05071999

関連ノート

読み込み中…