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Dichloromethane → 1-(3-Bromoprop-1-yn-1-yl)-4-chlorobenzene

HRID 2414575
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HRID 2414575 반응식
[Br:1][CH2:2][C:3]#[C:4][C:5]1[CH:10]=[CH:9][C:8](O)=[CH:7][CH:6]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.BrBr.[Cl:33]CCl>>[Br:1][CH2:2][C:3]#[C:4][C:5]1[CH:10]=[CH:9][C:8]([Cl:33])=[CH:7][CH:6]=1
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참가 물질

5

반응물 4

HCID 6344Dichloromethane2회HCID 11776TriphenylphosphineHCID 24408BromineHCID 226448974-(3-Bromoprop-1-YN-1-YL)phenol

생성물 1

HCID 105136071-(3-Bromoprop-1-yn-1-yl)-4-chlorobenzene수율 80%

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온도
0 °C

실험 절차

To a solution of 4-(3-bromo-prop-1-ynyl)-phenol (5.0 g, 30.12 mmol) dissolved in dichloromethane, 8.3 g (31.63 mmol, 1.05 eq) of triphenylphosphine was added and the solution was cooled to 0° C. Bromine (1.55 mL, 30.12 mmol, 1.0 eq) was added dropwise and the reaction was warmed to room temperature. The reaction was then diluted with dichloromethane, washed with sodium hydrosulfite pentahydrate, washed with brine, dried over MgSO4 and concentrated. The residue was purified via flash chromatography using 4:1 hexane:ethyl acetate to afford 5.56 g (80%) of 1-(3-bromo-prop-1-ynyl)-4-chloro-benzene as an amber oil. Electrospray Mass Spec 280.4 (M+H)+

후처리

  1. temperaturethe reaction was warmed to room temperature
  2. washwashed with sodium hydrosulfite pentahydrate
  3. washwashed with brine
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated
  6. customThe residue was purified via flash chromatography

출처 및 근거

ORD 기록
ord-7b2a6725032e42e49c5592a95d28a21a
출처 데이터셋
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06812227B2

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