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2,6-Difluoro-3-methoxybenzaldehyde → 2,6-Difluoro-3-methoxybenzyl alcohol

HRID 1486298
ノート
印刷プレビュー

反応式

HRID 1486298 の反応式
[F:1][C:2]1[C:9]([O:10][CH3:11])=[CH:8][CH:7]=[C:6]([F:12])[C:3]=1[CH:4]=[O:5].[BH4-].[Na+]>C(O)C>[F:1][C:2]1[C:9]([O:10][CH3:11])=[CH:8][CH:7]=[C:6]([F:12])[C:3]=1[CH2:4][OH:5]
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

4

反応物 2

HCID 5990732,6-Difluoro-3-methoxybenzaldehydeHCID 4311764Sodium borohydride

生成物 1

HCID 52448622,6-Difluoro-3-methoxybenzyl alcohol

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
0 °C

実験手順

A stirred solution of 600 mg (3.48 mmol) of 2,6-difluoro-3-methoxybenzaldehyde (CAS 149949-30-4) in 8 ml of ethanol at 0° C. was admixed with 65.9 mg (1.74 mmol) of sodium borohydride in portions. After stirring at 0° C. for 30 min, the reaction mixture was quenched with water and extracted three times with methyl tert-butyl ether. The combined organic extracts were washed with water and saturated aqueous sodium chloride solution, and dried with a phase separation cartridge. The solvent was drawn off to dryness under reduced pressure, which gave 550 mg (89% of theory) of the target compound.

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

後処理

  1. customat 0° C.
  2. customthe reaction mixture was quenched with water
  3. extractionextracted three times with methyl tert-butyl ether
  4. washThe combined organic extracts were washed with water and saturated aqueous sodium chloride solution
  5. customdried with a phase separation cartridge
  6. customgave 550 mg (89% of theory) of the target compound

出典と根拠

ORDレコード
ord-253c5a1b6bb64b3c92cb4432a038cc3b
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09422285B2

反応ノート

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