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Water → 2-Bromo-2,6-dichloro-6-fluorocyclohexanol

HRID 399332
ノート
印刷プレビュー

反応式

HRID 399332 の反応式
B(Br)(Br)[Br:2].[Cl:5][C:6]12O[CH:11]1[CH2:10][CH2:9][C:8]([Cl:14])([F:13])[CH2:7]2.[OH2:15]>ClCCl>[Br:2][C:6]1([Cl:5])[CH2:11][CH2:10][CH2:9][C:8]([Cl:14])([F:13])[CH:7]1[OH:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 25134Boron tribromideHCID 189709661,3-Dichloro-3-fluoro-7-oxabicyclo[4.1.0]heptane

生成物 1

HCID 189709682-Bromo-2,6-dichloro-6-fluorocyclohexanol

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

2.91 cm3 (2.91 mmol) of BBr3 in molar solution in dichloromethane were introduced at 4° C. under argon atmosphere into 0.98 (5.3 mmol) of epoxide 2e in solution in 6.5 cm3 dichloromethane. The reaction mixture was then allowed to return to room temperature and stirring was continued (1 h 30 min). 5 cm3 of distilled water were then added and the mixture was extracted with dichloromethane (4×10 cm3). The extract was dried over MgSO4, filtered and evaporated down. The crude product was purified by flash chromatography on silica (eluent ether/petroleum ether=5/95): 1.03 g of alcohol 1i were obtained (macrobore GC purity>97%); the yield of product 1i was 73%.

後処理

  1. customto return to room temperature
  2. custom(1 h 30 min)
  3. extractionthe mixture was extracted with dichloromethane (4×10 cm3)
  4. dry with materialThe extract was dried over MgSO4
  5. filtrationfiltered
  6. customevaporated down
  7. customThe crude product was purified by flash chromatography on silica (eluent ether/petroleum ether=5/95)

出典と根拠

ORDレコード
ord-9f1f4514115346af92551ecb861db111
出典データセット
uspto-grants-1998_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05817890

反応ノート

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