Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → Phenyl ethenesulfonate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Phenol | HCID 996 | — |
| 반응물 | Ethanesulfonylchloride, 2-chloro- | HCID 15385 | — |
| 반응물 | Vinylsulfonic acid | HCID 62474 | — |
| 생성물 | Phenyl ethenesulfonate | HCID 564920 | — |
반응 단계
The aryl ester of vinylsulfonic acid can be prepared by several available techniques. One method, described in U.S. Pat. No. 3,121,730 to Distler, involves reacting a beta-chloro-ethanesulfonic acid chloride with phenol in an aqueous medium at a pH of between 7.5 and 11.5. The reaction proceeds with a loss of 2 mols of hydrogen chloride to yield phenyl vinylsulfonate. An alternative method, described in U.S. Pat. No. 3,133,948, also to Distler, involves reacting carbyl sulfate with an aromatic hydroxy compound in an aqueous alkaline medium at a pH between 7.5 and 11.5 to yield a phenyl vinylsulfonate.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04122266 |
| 출처 데이터셋 | uspto-grants-1978_10 |
| ORD ID | ord-05dc6b88a69d4f28ba8be4b944e7c85d |
| 출처 메모 | uspto-grants-1978_10 |