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Benzyl Bromide → 2-(3-Benzyloxyphenoxy)ethanol

HRID 393359
ノート
印刷プレビュー

反応式

HRID 393359 の反応式
[OH:1][CH2:2][CH2:3][O:4][C:5]1[CH:11]=[CH:10][CH:9]=[C:7]([OH:8])[CH:6]=1.[OH-].[Na+].[CH2:14](Br)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>CO>[CH2:14]([O:8][C:7]1[CH:6]=[C:5]([CH:11]=[CH:10][CH:9]=1)[O:4][CH2:3][CH2:2][OH:1])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=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 7498Benzyl BromideHCID 14798Sodium HydroxideHCID 152273Phenol, 3-(2-hydroxyethoxy)-

生成物 1

HCID 121470482-(3-Benzyloxyphenoxy)ethanol収率 79.4%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of O-(2-Hydroxyethyl)resorcinol (4 g) and sodium hydroxide (1.04 g) dissolved in methanol (60 mL) was added benzyl bromide (4.44 g), and the resulting reaction mixture was stirred overnight. After this time, approximately 30 mL of the methanol was removed in vacuo, and the mixture was diluted with methylene chloride (100 mL). The organics were washed with water and aqueous 1N NaOH, dried, and concentrated to provide 2-(3-benzyloxyphenoxy)ethanol (5.03 g).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customthe resulting reaction mixture
  2. customAfter this time, approximately 30 mL of the methanol was removed in vacuo
  3. additionthe mixture was diluted with methylene chloride (100 mL)
  4. washThe organics were washed with water and aqueous 1N NaOH
  5. customdried
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-39e70c5d47ff499eb457287233bf9d7b
出典データセット
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06806369B2

反応ノート

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