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Water → N-(3-phenoxy)propionyl-prolinal

HRID 256153
ノート
印刷プレビュー

反応式

HRID 256153 の反応式
[O:1]([CH2:8][CH2:9][C:10]([N:12]1[CH2:18][CH2:17][CH2:16][C@H:13]1[CH2:14][OH:15])=[O:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(N(CC)CC)C.O>CS(C)=O>[O:1]([CH2:8][CH2:9][C:10]([N:12]1[CH2:18][CH2:17][CH2:16][C@H:13]1[CH:14]=[O:15])=[O:11])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
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 3

HCID 962WaterHCID 8471TriethylamineHCID 13932937N-(3-phenoxy)propionyl-prolinol

生成物 1

HCID 13932965N-(3-phenoxy)propionyl-prolinal収率 86.4%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒2 回

実験手順

A mixture of N-(3-phenoxy)propionyl-prolinol (1.4 g) and triethylamine (1.7 g) was dissolved in anhydrous dimethyl sulfoxide (16 ml), and to the stirred solution, a solution (16 ml) of sulfur trioxide-pyridine complex (2.6 g) in dimethyl sulfoxide was added. After stirring the mixture at room temperature for 10 minutes, the reaction solution was poured into iced water (150 ml) and subjected to extraction with ethyl acetate. The extract was washed successively with 10% aqueous citric acid, water, saturated aqueous sodium bicarbonate and brine, and dried over anhydrous magnesium sulfate. After distilling off the solvent under vacuum, the resulting crude product was purified by medium-pressure liquid column chromatography on silica gel (solvent: chloroform) to obtain the end compound as an oil (1.2 g).

後処理

  1. extractionsubjected to extraction with ethyl acetate
  2. washThe extract was washed successively with 10% aqueous citric acid, water, saturated aqueous sodium bicarbonate and brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. distillationAfter distilling off the solvent under vacuum
  5. customthe resulting crude product was purified by medium-pressure liquid column chromatography on silica gel (solvent: chloroform)

出典と根拠

ORDレコード
ord-9c6c0e839367433aaca8ffd8bd1e1972
出典データセット
uspto-grants-1987_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04701465

反応ノート

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