Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Water → 4-(Benzyloxy)benzene-1-sulfonyl chloride
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | Benzyl Phenyl Ether | HCID 70352 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 생성물 | 4-(Benzyloxy)benzene-1-sulfonyl chloride | HCID 4738385 | — |
반응 단계
To a suspension of 22.4 g (146 mmol) of sulfur trioxide/DMF complex in 60 mL of anhydrous 1,2-dichloroethane at room temperature, was added a solution of 30 g (162 mmol) of benzylphenyl ether in 30 mL of anhydrous 1,2-dichloroethane. The resulting mixture was warmed to reflux and maintained there for 1 hour, cooled to room temperature and 10.8 mL (146 mmol) of thionyl chloride added. The reaction was then warmed to 75 C for 1 hour, cooled in an ice bath, 50 mL of water slowly added, then ethyl acetate. The layers were separated, washed with saturated sodium bicarbonate, brine, dried with magnesium sulfate, filtered and stripped. The resulting solids were triturated with hexane to afford 24.5 g of pure 4-(Benzyloxy)benzenesulfonyl chloride.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06747027B1 |
| 출처 데이터셋 | uspto-grants-2004_06 |
| ORD ID | ord-be569f83d1ea421887b5ea785b7a15d0 |
| 출처 메모 | uspto-grants-2004_06 |