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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → 2-(4-Ethylbenzyl)phenol

HRID 1182030
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HRID 1182030 반응식
[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[O:16]C)=[CH:5][CH:4]=1)[CH3:2].B(Br)(Br)Br.O>ClCCl>[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[OH:16])=[CH:5][CH:4]=1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 25134Boron tribromideHCID 17964392(4-Ethylphenyl)(2-methoxyphenyl)methane

생성물 1

HCID 116585572-(4-Ethylbenzyl)phenol

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

0.83 g of (4-ethylphenyl)(2-methoxyphenyl)methane 55 is dissolved in dichloromethane. 11.0 ml of boron tribromide (1 M in CH2Cl2) are added dropwise to the mixture. The mixture is stirred at room temperature for 5 hours and, after addition of water, the dichloromethane phase is separated off. The aqueous phase is extracted with ethyl acetate. The combined organic phases are washed with water and NaCl solution, dried over sodium sulfate and concentrated. 0.77 g is obtained as crude product which can be purified by chromatography. C15H16O (212.29) MS (ESI): 235.20 (M+Na+)

후처리

  1. customthe dichloromethane phase is separated off
  2. extractionThe aqueous phase is extracted with ethyl acetate
  3. washThe combined organic phases are washed with water and NaCl solution
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated
  6. custom0.77 g is obtained as crude product which
  7. customcan be purified by chromatography

출처 및 근거

ORD 기록
ord-beda1aab79724a5890a4e1c56d86d2e5
출처 데이터셋
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07288528B2

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