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

HRID 2414575
ノート
印刷プレビュー

反応式

HRID 2414575 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 6344Dichloromethane2 回HCID 11776TriphenylphosphineHCID 24408BromineHCID 226448974-(3-Bromoprop-1-YN-1-YL)phenol

生成物 1

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

反応条件

温度
0 °C

実験手順

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)+

後処理

  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

出典と根拠

ORDレコード
ord-7b2a6725032e42e49c5592a95d28a21a
出典データセット
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06812227B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート