HCID 66733858、化合物 → HCID 66733586、化合物

HRID 1929621ノート

反応式

HRID 1929621 の反応式
C([O:5][C:6](=O)[CH2:7][CH2:8][C:9]1[CH:14]=[C:13]([F:15])[C:12]([CH3:16])=[C:11]([F:17])[CH:10]=1)CCC>C1COCC1>[F:15][C:13]1[CH:14]=[C:9]([CH2:8][CH2:7][CH2:6][OH:5])[CH:10]=[C:11]([F:17])[C:12]=1[CH3:16]

参加物

3

反応条件

温度
0 °C

実験手順

To an ice-cooled solution of 3-(3,5-difluoro-4-methyl-phenyl)-propionic acid butyl ester (2.200 g; 8.584 mmol) in anhydrous THF (20 ml) was added dropwise a 1N solution of BH3.THF complex in THF (13 ml; 13 mmol). The resulting solution was stirred at 0° C., under nitrogen, for 1 h, and then at rt overnight. The reaction mixture was quenched by dropwise addition of MeOH (5 ml) followed by water (10 ml). The volatiles were removed under vacuum, and the product was extracted with DCM (3×20 ml). The combined organic layers were then washed with brine, dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure. The crude was purified by FC (DCM/MeOH=12/1) to give the pure product 3-(3,5-difluoro-4-methyl-phenyl)-propan-1-ol as a pale yellow oil (1.440 g; 90%). LC-MS: tR=0.87 min.; [M+H]+: no ionisation.

後処理

  1. customat rt
  2. customovernight
  3. customThe reaction mixture was quenched by dropwise addition of MeOH (5 ml)
  4. customThe volatiles were removed under vacuum
  5. extractionthe product was extracted with DCM (3×20 ml)
  6. washThe combined organic layers were then washed with brine
  7. dry with materialdried over anh. MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated to dryness under reduced pressure
  10. customThe crude was purified by FC (DCM/MeOH=12/1)

出典と根拠

ORDレコード
ord-9b12885abb4e49caa224f9245b6868f9
出典データセット
uspto-grants-2012_05
特許番号
US08188082B2

反応ノート

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