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Triethylamine → 4-Bromo-1-methyl-2-phenoxybenzene

HRID 1430250
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인쇄 미리보기

반응식

HRID 1430250 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:9])=[C:6]([OH:8])[CH:7]=1.[C:10]1(B(O)O)[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.C(N(CC)CC)C>ClCCl.C(OCC)(=O)C.CC([O-])=O.CC([O-])=O.[Cu+2]>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:9])=[C:6]([O:8][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 8471TriethylamineHCID 66827Phenylboronic AcidHCID 126484045-Bromo-2-methylphenol

생성물 1

HCID 542867314-Bromo-1-methyl-2-phenoxybenzene

시약·촉매·용매 3

HCID 8895Cupric acetate촉매HCID 6344Dichloromethane용매

실험 절차

A mixture of 5-bromo-2-methylphenol (1.0 g), phenylboronic acid (1.30 g), Cu(OAc)2 (0.97 g), and triethylamine (2.98 mL) in dichloromethane (50 mL) was stirred for 4 days. The mixture was diluted with ethyl acetate, washed four times with 1M aqueous NaOH solution and once with brine, dried over Na2SO4, filtered, and concentrated. The crude product was chromatographed on silica gel using 2% ethyl acetate in hexanes to afford the title compound.

후처리

  1. washwashed four times with 1M aqueous NaOH solution
  2. dry with materialonce with brine, dried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe crude product was chromatographed on silica gel using 2% ethyl acetate in hexanes

출처 및 근거

ORD 기록
ord-4f27d8df278e4efeab4bfa02028cf45f
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08940737B2

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이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 8857
Ethyl Acetate
용매