Water → N-(tert-Butoxycarbonyl)-D-prolinal

HRID 359470

反応式

HRID 359470 の反応式
O.[OH:2][CH2:3][C@H:4]1[CH2:8][CH2:7][CH2:6][N:5]1[C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10]>C(Cl)Cl.[Cr](Cl)([O-])(=O)=O.[NH+]1C=CC=CC=1>[CH:3]([C@H:4]1[CH2:8][CH2:7][CH2:6][N:5]1[C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])=[O:2]

参加物

5

反応物 2

HCID 962WaterHCID 688279N-(tert-Butoxycarbonyl)-D-prolinol

生成物 1

HCID 7009153N-(tert-Butoxycarbonyl)-D-prolinal収率 102%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 178418287HCID 178418287、化合物溶媒

反応条件

温度
25 °C

実験手順

To a water cooled (25° C.) solution of 10.0 g of (R)-2-(hydroxymethyl)-1-pyrrolidinecarboxylic acid, 1,1-dimethylethyl ester in 250 ml of dry methylene chloride is added in one portion 16.0 g of pyridinium chlorochromate, 36.0 g of dried, crushed 4Å molecular sieves and 4.5 ml of glacial acetic acid. The resulting mixture is stirred at 25° C. for one hour. Twenty-five grams of diatomaceous earth and 500 ml of diethyl ether is added, the suspension is filtered through a pad of diatomaceous earth and the filtrate concentrated in vacuo. The residue is dissolved in diethyl ether and is passed through a short column of silica gel using diethyl ether as the eluant. The first two 500 ml fractions contain the desired aldehyde. The solvent is concentrated in vacuo to give 10.1 g of desired product.

後処理

  1. custom36.0 g of dried
  2. customcrushed 4Å molecular sieves and 4.5 ml of glacial acetic acid
  3. additionTwenty-five grams of diatomaceous earth and 500 ml of diethyl ether is added
  4. filtrationthe suspension is filtered through a pad of diatomaceous earth
  5. concentrationthe filtrate concentrated in vacuo
  6. dissolutionThe residue is dissolved in diethyl ether
  7. concentrationThe solvent is concentrated in vacuo

出典と根拠

ORDレコード
ord-8639a42bff00433bb8550db28372ba6d
出典データセット
uspto-grants-1991_03
特許番号
US05001142

関連ノート

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