Benzyl Alcohol → (5-Benzyloxy-2-chloro-phenyl)-acetic acid

HRID 1810529ノート

反応式

HRID 1810529 の反応式
[CH2:1]([OH:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Na+].[Cl:11][C:12]1[CH:17]=[CH:16][C:15](F)=[CH:14][C:13]=1[CH2:19][C:20]([OH:22])=[O:21]>CN1C(=O)CCC1>[CH2:1]([O:8][C:15]1[CH:16]=[CH:17][C:12]([Cl:11])=[C:13]([CH2:19][C:20]([OH:22])=[O:21])[CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

5

反応物 3

HCID 244Benzyl AlcoholHCID 24758Sodium hydrideHCID 35354302-(2-Chloro-5-fluorophenyl)acetic acid

生成物 1

HCID 58149280(5-Benzyloxy-2-chloro-phenyl)-acetic acid

試薬・触媒・溶媒 1

HCID 13387N-methyl-2-pyrrolidone溶媒

実験手順

To benzyl alcohol (1.1 g, 10 mmol) in NMP (20 mL) was added sodium hydride (60% in mineral oil; 0.44 g, 11 mmol), and the mixture was stirred for 30 minutes at room temperature. The mixture was then added to a vial containing 2-chloro-5-fluorophenylacetic acid (1 g, 4.5 mmol), and the reaction was stirred at 120° C. for 3 hours. Acidic work-up gave the title compound.

後処理

  1. additionThe mixture was then added to
  2. stirringthe reaction was stirred at 120° C. for 3 hours

出典と根拠

ORDレコード
ord-c1875ad230ab4d3aac436f9491af7b30
出典データセット
uspto-grants-2013_01
特許番号
US08362044B2

反応ノート

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