Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Hydroxybenzenesulfonic acid → 4-(Chlorosulfonyl)phenyl acetate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Hydroxybenzenesulfonic acid | HCID 4765 | — |
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | Oxalyl chloride | HCID 65578 | — |
| 촉매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | 4-(Chlorosulfonyl)phenyl acetate | HCID 12925710 | 83% |
반응 단계
6.285 g (36.08 mmol) of 4-hydroxybenzenesulfonic acid was dissolved in a mixture of 30 mL of acetic anhydride and 15 mL of acetic acid and refluxed for 6 hours. The volatiles were evaporated and placed under high vacuum overnight. The resulting crude product was dissolved in 100 mL of DCM and treated with 4.72 mL of oxalyl chloride (54.12 mmol) and 139 μL of DMF (1.804 mmol) at 0° C. Stirring was continued until gas evolution ceased then the reaction was concentrated and re-dissolved in EtOAc. The organic layer was washed twice with 2 N H2SO4, and dried with brine and MgSO4. concentration gave 7.067 g of 4-(chlorosulfonyl)phenyl acetate as a dark thick oil that eventually solidified (83% yield over two steps).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07939671B2 |
| 출처 데이터셋 | uspto-grants-2011_05 |
| ORD ID | ord-b9587f49887b419990d29c2de45853d0 |
| 출처 메모 | uspto-grants-2011_05 |