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Phosphorus tribromide → 3-(Bromomethyl)-2,4-difluorophenol

HRID 1179273
ノート
印刷プレビュー

反応式

HRID 1179273 の反応式
[F:1][C:2]1[C:7]([CH2:8]O)=[C:6]([F:10])[CH:5]=[CH:4][C:3]=1[OH:11].P(Br)(Br)[Br:13]>C(OCC)C>[Br:13][CH2:8][C:7]1[C:2]([F:1])=[C:3]([OH:11])[CH:4]=[CH:5][C:6]=1[F:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24614Phosphorus tribromideHCID 451191212,4-Difluoro-3-(hydroxymethyl)phenol

生成物 1

HCID 692645783-(Bromomethyl)-2,4-difluorophenol収率 47%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

To a stirred solution of 2,4-difluoro-3-(hydroxymethyl)phenol (step 1, 410 mg, 256 mmol) in diethyl ether (4 mL) and dichloromethne (1 mL) was added phosphorus tribromide (0.257 mL, 2.71 mmol) at 0° C. The mixture was stirred for 30 min, and then the mixture was poured onto ice-aqueous sodium bicarbonate. The mixture was extracted with ethyl acetate (200 mL), and the organic layer was washed with water and brine, dried over magnesium sulfate and evapolated to afford 266 mg (47%) of the title compound as a colorless oil, which was used in the next step without purification:

後処理

  1. additionthe mixture was poured onto ice-aqueous sodium bicarbonate
  2. extractionThe mixture was extracted with ethyl acetate (200 mL)
  3. washthe organic layer was washed with water and brine
  4. dry with materialdried over magnesium sulfate

出典と根拠

ORDレコード
ord-24398224da1845f48aca480044b72774
出典データセット
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07279486B2

反応ノート

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