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Sodium borohydride → 2-Methoxymethoxy-5-(trifluoromethyl)benzyl alcohol

HRID 1081875
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HRID 1081875 반응식
[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:12]=[CH:11][C:10]([C:13]([F:16])([F:15])[F:14])=[CH:9][C:6]=1[CH:7]=[O:8].[BH4-].[Na+]>CO>[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:12]=[CH:11][C:10]([C:13]([F:14])([F:15])[F:16])=[CH:9][C:6]=1[CH2:7][OH:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 233631132-(Methoxymethoxy)-5-(trifluoromethyl)benzaldehyde

생성물 1

HCID 543883822-Methoxymethoxy-5-(trifluoromethyl)benzyl alcohol수율 95%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

The solution of 2-methoxymethoxy-5-(trifluoromethyl)benzaldehyde (3.3 g) from Example 59 in anhydrous methanol (20 ml) was cooled in an ice bath, followed by gradual addition of NaBH4 (0.53 g). After stirring at room temperature for 15 minutes, the solvent was removed under reduced pressure. To the residue was added water, and the aqueous layer was extracted with ether. The ether layer was washed with water and saturated sodium chloride solution, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, to give an colorless oil compound as the title compound (3.15 g; 95%).

후처리

  1. customthe solvent was removed under reduced pressure
  2. additionTo the residue was added water
  3. extractionthe aqueous layer was extracted with ether
  4. washThe ether layer was washed with water and saturated sodium chloride solution
  5. dry with materialdried over anhydrous sodium sulfate
  6. customThe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-5890f8f66af04e2d9ebcf9b627454dbe
출처 데이터셋
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05587392

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