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

HRID 1081875
ノート
印刷プレビュー

反応式

HRID 1081875 の反応式
[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]
参加物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 4311764Sodium borohydrideHCID 233631132-(Methoxymethoxy)-5-(trifluoromethyl)benzaldehyde

生成物 1

HCID 543883822-Methoxymethoxy-5-(trifluoromethyl)benzyl alcohol収率 95%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

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%).

後処理

  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

出典と根拠

ORDレコード
ord-5890f8f66af04e2d9ebcf9b627454dbe
出典データセット
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05587392

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート