돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 389001생성일: 2026년 10월 26일

Water → Triphenylsulfonium (8-hydroxyoctyloxycarbonyl)difluoromethanesulfonate

https://huagongshe.com/reaction/389001

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물ChlorobenzeneHCID 7964—
반응물TetrahydrofuranHCID 8028—
반응물1,8-OctanediolHCID 69420—
반응물Diphenylammonium TrifluoromethanesulfonateHCID 11209371—
생성물Triphenylsulfonium (8-hydroxyoctyloxycarbonyl)difluoromethanesulfonateHCID 86613395—

반응 단계

30.0 parts of TPS-1, 20.0 parts of octane-1,8-diol, 2.2 parts of diphenylammonium triflate and 210 parts of monochlorobenzene were mixed and the resultant mixture was stirred at 80° C. to effect reaction. After completion of the reaction, the reaction mixture was concentrated to remove monochlorobenzene. Chloroform was added to the concentrate obtained and ion-exchanged water was added thereto. A chloroform layer was separated. After repeatedly washing the chloroform layer with ion-exchange water, 4.2 parts of active carbon was added to the chloroform layer obtained to stir for 1 hour. The chloroform layer was filtered and concentrated to obtain pale yellow oily matters. Tetrahydrofuran was added to the oily matters to stir. The mixture was filtered and the filtrate obtained was concentrated. Ethyl acetate was added to the concentrate obtained and the resultant mixture was stirred to conduct decantation. After repeating this operation, the residue was concentrated to obtain 19.5 parts of triphenylsulfonium (8-hydroxyoctyloxycarbonyl)difluoromethanesulfonate in the form of pale yellow oil, which is called as TPS-5.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08378016B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-08479d599718413db41663352c3ef200
출처 메모uspto-grants-2013_02