Phosphorus tribromide → 1-Bromo-4-(1-bromoethyl)benzene

HRID 1525861ノート

反応式

HRID 1525861 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8](O)[CH3:9])=[CH:4][CH:3]=1.P(Br)(Br)[Br:12]>ClCCl>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([Br:12])[CH3:9])=[CH:4][CH:3]=1

参加物

4

実験手順

A solution of 1-(4-bromophenyl)ethanol (1.492 mmol) in dichloromethane (8 mL) at 0° C. was treated dropwise with a solution of phosphorous tribromide (0.597 mmol) in dichloromethane (2 mL). The reaction was allowed to warm to room temperature and was stirred overnight. The reaction was then quenched with saturated aq sodium bicarbonate (10 mL) and was stirred for 2 h. The biphasic mixture was further diluted with dichloromethane (50 mL) and the organic layer was separated from the aqueous layer. The organic layer was dried over sodium sulfate, filtered and concentrated to dryness in vacuo. Purification of the residue by flash chromatography (0-25% ethyl acetate/hexanes) gave the title product (91 mg, 23% yield) as a clear oil. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.97 (d, J=6.82 Hz, 3 H) 5.50 (q, J=6.82 Hz, 1 H) 7.48 (d, J=8.59 Hz, 2 H) 7.57 (m, J=8.59 Hz, 2 H).

後処理

  1. customThe reaction was then quenched with saturated aq sodium bicarbonate (10 mL)
  2. stirringwas stirred for 2 h
  3. additionThe biphasic mixture was further diluted with dichloromethane (50 mL)
  4. customthe organic layer was separated from the aqueous layer
  5. dry with materialThe organic layer was dried over sodium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated to dryness in vacuo
  8. customPurification of the residue by flash chromatography (0-25% ethyl acetate/hexanes)

出典と根拠

ORDレコード
ord-489d8f1c6fca4f1cb75ca8e42e50fe4c
出典データセット
uspto-grants-2015_07
特許番号
US09084794B2

反応ノート

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