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2-(Trifluoromethoxy)benzoic acid → 2-(Trifluoromethoxy)benzyl alcohol

HRID 1740592
ノート
印刷プレビュー

反応式

HRID 1740592 の反応式
[F:1][C:2]([F:14])([F:13])[O:3][C:4]1[CH:12]=[CH:11][CH:10]=[CH:9][C:5]=1[C:6](O)=[O:7]>C1COCC1>[F:1][C:2]([F:13])([F:14])[O:3][C:4]1[CH:12]=[CH:11][CH:10]=[CH:9][C:5]=1[CH2:6][OH:7]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 27772232-(Trifluoromethoxy)benzoic acid

生成物 1

HCID 27772452-(Trifluoromethoxy)benzyl alcohol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a stirred solution of 2-trifluoromethoxybenzoic acid (1.0 g, 5.2 mmol) in THF (25 mL) at 0° C. was added borane-THF complex (15 mL of a 1.0 M solution in THF, 15 mmol). The solution was warmed to ambient temperature and stirred for 14 h. The solvent was removed under reduced pressure and the residue was partitioned between EtOAc (75 mL) and saturated aqueous NaHCO3 (75 mL). The organic phase was dried (MgSO4), filtered and the solvent was removed under reduced pressure to give 2-trifluoromethoxybenzyl alcohol as a colorless liquid (TLC Rf =0.2 (1:3 EtOAc-hexanes)).

後処理

  1. customThe solvent was removed under reduced pressure
  2. customthe residue was partitioned between EtOAc (75 mL) and saturated aqueous NaHCO3 (75 mL)
  3. dry with materialThe organic phase was dried (MgSO4)
  4. filtrationfiltered
  5. customthe solvent was removed under reduced pressure

出典と根拠

ORDレコード
ord-cc76186cf83940e79fb194eed7bb111c
出典データセット
uspto-grants-1999_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05968938

反応ノート

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