3-(Phenylmethoxy)benzenemethanol → 3-Benzyloxybenzyl bromide

HRID 725022

反応式

HRID 725022 の反応式
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:14]=[CH:15][CH:16]=1)[CH2:12]O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Si]([Br:21])(C)(C)C>C(Cl)Cl>[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:14]=[CH:15][CH:16]=1)[CH2:12][Br:21])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

4

反応物 2

HCID 743413-(Phenylmethoxy)benzenemethanolHCID 76113Bromotrimethylsilane

生成物 1

HCID 15020473-Benzyloxybenzyl bromide

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A solution of 3-benzyloxybenzyl alcohol (2.04 g) in methylene chloride (20 mL) with TMS Bromide (2.5 eq. 3.14 mL) was heated at reflux for 6 hr. After cooling, the reaction was concentrated and then reconcentrated 2× from methylene chloride. The residue was chromatographed on silica gel with 5% methylene chloride in hexane to afford 3-benzyloxybenzyl bromide (1.26 g) as an oil.

後処理

  1. temperatureat reflux for 6 hr
  2. temperatureAfter cooling
  3. concentrationthe reaction was concentrated
  4. customThe residue was chromatographed on silica gel with 5% methylene chloride in hexane

出典と根拠

ORDレコード
ord-148bdd1a9f154f59962ee4b9f4440268
出典データセット
uspto-grants-1998_01
特許番号
US05705524

関連ノート

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