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

HRID 1486298
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HRID 1486298 반응식
[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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

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

생성물 1

HCID 52448622,6-Difluoro-3-methoxybenzyl alcohol

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
0 °C

실험 절차

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.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  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

출처 및 근거

ORD 기록
ord-253c5a1b6bb64b3c92cb4432a038cc3b
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09422285B2

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