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4-Methyloxybenzyl chloride → HCID 11095877、化合物

HRID 989924
ノート
印刷プレビュー

反応式

HRID 989924 の反応式
[OH:1][C@@H:2]([CH3:6])[C:3]([OH:5])=[O:4].CC(C)([O-])C.[K+].[CH3:13][O:14][C:15]1[CH:22]=[CH:21][C:18]([CH2:19]Cl)=[CH:17][CH:16]=1>CN(C=O)C>[OH:1][C@@H:2]([CH3:6])[C:3]([O:5][CH2:19][C:18]1[CH:21]=[CH:22][C:15]([O:14][CH3:13])=[CH:16][CH:17]=1)=[O:4]
参加物反応条件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 699934-Methyloxybenzyl chlorideHCID 107689L-Lactic AcidHCID 23665647Potassium tert-butoxide

生成物 1

HCID 11095877HCID 11095877、化合物

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
25 °C

実験手順

To a stirred solution of (S)(+)-2 hydroxypropionic acid (9.0 g, 100 mmole) in 100 ml dry DMF was added potassium tert-butoxide (12.34 g, 110 mmole) and the mixture was stirred for one hour at 25° C. 4Methoxybenzyl chloride (18.8 g 120 mmole) was added and the mixture was stirred for six hours at 60° C. The mixture was evaporated under reduced pressure and 250 ml ethyl acatate was added. The organic phase was washed four times with water. The organic phase was dried with sodium sulfate and concentrated in vacuo. Yield: 15.6 g=74%

後処理

  1. stirringthe mixture was stirred for six hours at 60° C
  2. customThe mixture was evaporated under reduced pressure and 250 ml ethyl acatate
  3. additionwas added
  4. washThe organic phase was washed four times with water
  5. dry with materialThe organic phase was dried with sodium sulfate
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-19c413e113a94f7bb5c0181f0e129f86
出典データセット
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06458772B1

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート