Chlorosulfonic acid → 4-(Oxazol-4-yl)benzene-1-sulfonyl chloride

HRID 1944710

反応式

HRID 1944710 の反応式
[C:1]1([C:7]2[N:8]=[CH:9][O:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cl:12][S:13](O)(=[O:15])=[O:14]>ClCCl>[O:10]1[CH:11]=[C:7]([C:1]2[CH:2]=[CH:3][C:4]([S:13]([Cl:12])(=[O:15])=[O:14])=[CH:5][CH:6]=2)[N:8]=[CH:9]1

参加物

4

反応物 2

HCID 24638Chlorosulfonic acidHCID 5892794-Phenyl-1,3-oxazole2 回

生成物 1

HCID 513419514-(Oxazol-4-yl)benzene-1-sulfonyl chloride収率 23%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
2.5 °C

実験手順

4-Phenyl-oxazole (Intermediate 25, 550 mg, 3.79 mmol) was dissolved in a minimum of dichloromethane and was added slowly to chlorosulfonic acid (2.537 mL, 37.9 mmol) at 0° C. The reaction mixture was stirred for 20 min 0-5° C. then warmed to room temperature then to 45° C. and stirred for 2 h. The reaction mixture was cooled to room temperature and cautiously poured on ice water. The aqueous layer was extracted with ethyl acetate, dried over sodium sulfate, and concentrated to crude 4-oxazol-4-yl-benzenesulfonyl chloride. The starting material and product have Rf values in 20% EtOAc/heptane of Rf=0.47 and Rf=0.23, respectively. The crude product was purifed by chromatography on a Biotage 25M column eluting ethyl acetate/heptane to yield 4-oxazol-4-yl-benzenesulfonyl chloride (212 mg, 0.870 mmol). MH+=244.2.

後処理

  1. temperaturethen warmed to room temperature
  2. stirringto 45° C. and stirred for 2 h
  3. temperatureThe reaction mixture was cooled to room temperature
  4. additioncautiously poured on ice water
  5. extractionThe aqueous layer was extracted with ethyl acetate
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated to crude 4-oxazol-4-yl-benzenesulfonyl chloride
  8. washeluting ethyl acetate/heptane

出典と根拠

ORDレコード
ord-71827a9a67b2463dbe437185ac6aa80e
出典データセット
uspto-grants-2013_03
特許番号
US08394858B2

関連ノート

読み込み中…