돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1702443생성일: 2026년 10월 26일

Pyridine → beta,beta,beta-Trichloroethoxycarbonylsulfenyl Chloride

https://huagongshe.com/reaction/1702443

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물DichloromethaneHCID 6344—
반응물(Chlorothio)formyl chlorideHCID 75990—
반응물1,1,2-TrichloroethanolHCID 119427—
생성물beta,beta,beta-Trichloroethoxycarbonylsulfenyl ChlorideHCID 12878643—

반응 단계

To an ice cold vigorously stirred (mechanical stirrer) solution of trichloroethanol (50.0 ml, 0.52 mol) and pyridine (42.0 ml, 0.52 mol) in 300 ml of methlene chloride, chlorocarbonylsulfenyl chloride (43.5 ml, 0.52 mol) was added dropwise over 30 min. After the addition the solution was stirred at 0° for 1.5 hr. The ice bath was removed and the stirring continued for 1.5 hr. The mixture (solid formed) was washed with ice- H2O and ice cold sat. NaCl. The organic layer was dried (MgSO4) and the solvent removed under reduced pressure. After removal of the solvent an oily solid remained. The solid was removed by triterration with ether and filtration of the solid. The filtrate was condensed under reduced pressure and the process repeated until, after removal of the solvent from the filtrate, the liquid could be filtered without the aid of solvent. The yellow liquid was distilled under reduced pressure: bp 54°-59° (0.25 mm; bath temp. 80°-90°); NMR(CDCl3)δ 5.0 (S, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04381300
출처 데이터셋uspto-grants-1983_04
ORD IDord-c8624f13b0e249ec928ba730dc6e5bb1
출처 메모uspto-grants-1983_04