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(Bis(2-methoxyethyl)amino)sulfur trifluoride → 4-Bromo-1-chloro-2-(1-fluoroethyl)benzene

HRID 245271
ノート
印刷プレビュー

反応式

HRID 245271 の反応式
COCCN(S(F)(F)[F:11])CCOC.[Br:14][C:15]1[CH:16]=[CH:17][C:18]([Cl:24])=[C:19]([CH:21](O)[CH3:22])[CH:20]=1>ClCCl.O>[Br:14][C:15]1[CH:16]=[CH:17][C:18]([Cl:24])=[C:19]([CH:21]([F:11])[CH3:22])[CH:20]=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 2

HCID 2734690(Bis(2-methoxyethyl)amino)sulfur trifluorideHCID 587626441-(5-Bromo-2-chlorophenyl)ethanol

生成物 1

HCID 591269474-Bromo-1-chloro-2-(1-fluoroethyl)benzene収率 65.8%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

Bis(2-methoxyethyl)aminosulfur trifluoride (4.5 g, 20.34 mmol) was added to a stirred solution of 1-(5-bromo-2-chlorophenyl)ethanol (3.99 g, 16.95 mmol) in dichloromethane (50 mL) at 0° C. The resulting solution was stirred at 0° C. for 3 h. The reaction mixture was quenched with a 5% solution of aqueous sodium bicarbonate (100 mL) and the resulting bubbling biphasic reaction mixture was vigorously stirred at 0° C. for 15 min. The reaction mixture was diluted with water (50 mL) and extracted with dichloromethane twice. The combined organic layers were washed with 1M hydrochloric acid, dried and concentrated by rotary evaporation. The product was purified by flash chromatography on silica gel (hexanes) to yield the title compound (2.65 g, 11.16 mmol, 65.8% yield) as a clear oil: 1H NMR (CDCl3) δ 7.65 (d, 1H), 7.37 (m, 1H), 7.20 (m, 1H), 5.88 (dq, 1H), 1.61 (dd, 3H).

後処理

  1. customThe reaction mixture was quenched with a 5% solution of aqueous sodium bicarbonate (100 mL)
  2. customthe resulting bubbling
  3. custombiphasic reaction mixture
  4. stirringwas vigorously stirred at 0° C. for 15 min
  5. extractionextracted with dichloromethane twice
  6. washThe combined organic layers were washed with 1M hydrochloric acid
  7. customdried
  8. concentrationconcentrated by rotary evaporation
  9. customThe product was purified by flash chromatography on silica gel (hexanes)

出典と根拠

ORDレコード
ord-a272d6206e164cd8bf2782c465e6bf64
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08658791B2

反応ノート

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