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Benzyl Bromide → 2-(3-Benzyloxyphenoxy)ethanol

HRID 393359
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HRID 393359 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7498Benzyl BromideHCID 14798Sodium HydroxideHCID 152273Phenol, 3-(2-hydroxyethoxy)-

생성물 1

HCID 121470482-(3-Benzyloxyphenoxy)ethanol수율 79.4%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

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).

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후처리

  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

출처 및 근거

ORD 기록
ord-39e70c5d47ff499eb457287233bf9d7b
출처 데이터셋
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06806369B2

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