돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1112470생성일: 2026년 10월 26일

Hydrochloric Acid → Phenyl ethenesulfonate

https://huagongshe.com/reaction/1112470

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물PhenolHCID 996—
반응물Ethanesulfonylchloride, 2-chloro-HCID 15385—
반응물Vinylsulfonic acidHCID 62474—
생성물Phenyl ethenesulfonateHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04122266
출처 데이터셋uspto-grants-1978_10
ORD IDord-05dc6b88a69d4f28ba8be4b944e7c85d
출처 메모uspto-grants-1978_10