4-Fluoro-3-(phenylmethoxy)benzenemethanol → 3-(Benzyloxy)-4-fluorobenzaldehyde

HRID 2389340ノート

反応式

HRID 2389340 の反応式
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH2:16][OH:17])[CH:12]=[CH:13][C:14]=1[F:15])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>C(Cl)Cl.[O-2].[O-2].[Mn+4]>[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:12]=[CH:13][C:14]=1[F:15])[CH:16]=[O:17])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

参加物

4

反応物 1

HCID 5614404-Fluoro-3-(phenylmethoxy)benzenemethanol

生成物 1

HCID 5613353-(Benzyloxy)-4-fluorobenzaldehyde収率 93.7%

試薬・触媒・溶媒 2

HCID 178418406HCID 178418406、化合物触媒HCID 6344Dichloromethane溶媒

実験手順

To a stirring solution of [3-(benzyloxy)-4-fluorophenyl]methanol (14 mg) in DCM (0.7 mL) was added manganese dioxide (140 mg) at ambient temperature. After 22 hours, the reaction mixture was filtered through a bed of Celite and evaporated in vacuo. The residue was purified by silica gel column chromatography (n-hexane:EtOAc=10:1) to give 3-(benzyloxy)-4-fluorobenzaldehyde (13 mg).

後処理

  1. filtrationthe reaction mixture was filtered through a bed of Celite
  2. customevaporated in vacuo
  3. customThe residue was purified by silica gel column chromatography (n-hexane:EtOAc=10:1)

出典と根拠

ORDレコード
ord-5dc314935a024a769c784718ca4e337b
出典データセット
uspto-grants-2012_09
特許番号
US08273745B2

反応ノート

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