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Ethanol → (3-(5-Methyl-thiophen-2-ylmethyl)-phenyl)-methanol

HRID 1927274
ノート
印刷プレビュー

反応式

HRID 1927274 の反応式
C(O)C.[CH3:4][C:5]1[S:9][C:8]([CH2:10][C:11]2[CH:12]=[C:13]([CH:16]=[CH:17][CH:18]=2)[CH:14]=[O:15])=[CH:7][CH:6]=1.[BH4-].[Na+]>O>[CH3:4][C:5]1[S:9][C:8]([CH2:10][C:11]2[CH:12]=[C:13]([CH2:14][OH:15])[CH:16]=[CH:17][CH:18]=2)=[CH:7][CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 702EthanolHCID 4311764Sodium borohydrideHCID 592873823-(5-Methyl-thiophen-2-ylmethyl)-benzaldehyde

生成物 1

HCID 59287391(3-(5-Methyl-thiophen-2-ylmethyl)-phenyl)-methanol収率 84.9%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a solution of ethanol (5.0 mL) and 3-(5-methyl-thiophen-2-ylmethyl)-benzaldehyde (350 mg) described in Manufacturing Example 52-2 was added sodium borohydride (120 mg), which was stirred for 10 minutes at room temperature. Water was added to the reaction solution, which was then extracted with ethyl acetate. The solvent was evaporated from the organic layer under a reduced pressure, and the residue was purified by silica gel chromatography (heptane:ethyl acetate=2:1) to obtain the titled compound (300 mg).

後処理

  1. extractionwas then extracted with ethyl acetate
  2. customThe solvent was evaporated from the organic layer under a reduced pressure
  3. customthe residue was purified by silica gel chromatography (heptane:ethyl acetate=2:1)

出典と根拠

ORDレコード
ord-6b304798ff4a446cace12547705eb42e
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08183264B2

反応ノート

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