beta-(p-Chlorophenyl)propionic acid → 4-Chlorobenzenepropanol

HRID 465862

反応式

HRID 465862 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][C:10](O)=[O:11])=[CH:4][CH:3]=1.B.O1CCCC1>O1CCCC1>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][CH2:10][OH:11])=[CH:6][CH:7]=1

参加物

4

実験手順

To a stirred solution of 5.0 g (27 mmol) of 3-(4-chlorophenyl)propionic acid in 30 ml of tetrahydrofuran at 0° C., 30 ml (1M in THF, 30 mmol) of borane-tetrahydrofuran solution was added dropwise. The reaction was stirred for 15 hours. The reaction mixture was concentrated in vacuo. The residue was quenched with water and partitioned between diethyl ether and saturated sodium bicarbonate. The organic layer was separated and the aqueous layer was extracted twice with 40 ml of diethyl ether. The organic layers were combined and washed with brine, dried over MgSO4 and concentrated in vacuo to obtain 3.9 g of a colorless oil.

後処理

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. customThe residue was quenched with water
  3. custompartitioned between diethyl ether and saturated sodium bicarbonate
  4. customThe organic layer was separated
  5. extractionthe aqueous layer was extracted twice with 40 ml of diethyl ether
  6. washwashed with brine
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-94e509240ef649b7855094cdaca12e72
出典データセット
uspto-grants-1992_10
特許番号
US05153327

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