돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 327682생성일: 2026년 10월 24일

Pyridine → 2-(4-Chlorophenoxy)ethanol sulfamate

https://huagongshe.com/ko/reaction/327682

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물2-(4-Chlorophenoxy)ethanolHCID 15907—
반응물N-Methylsulfamoyl chlorideHCID 11789235—
용매DichloromethaneHCID 6344—
생성물2-(4-Chlorophenoxy)ethanol sulfamateHCID 1910866735.3%

반응 단계

To a stirred solution of 45.0 g (0.347 mole) of methylsulfamoyl chloride prepared above in 100 ml of methylene chloride was added in a thin stream a solution of 25.0 g (0.145 mole) of 2-(4-chlorophenoxy)ethanol (Lancaster Synthesis, Inc., Windham, N.H. 03087) in 30 ml (0.369 mole) of pyridine and 100 ml of methylene chloride and the reaction mixture was stirred at ambient temperature for 3 days. The solids were removed by filtration and the filtrate was evaporated under reduced pressure to yield a brown viscous residue. The residue was partitioned between water and ethyl ether (400 ml each). The organic layer was washed twice with 300 ml portions of water, dried over magnesium sulfate (MgSO4) and the solvent evaporated under reduced pressure to yield a solid residue. The solid was triturated with 100 ml of isopropyl ether and the solid was recollected by filtration. The solid was recrystallized from isopropyl ether to give 12.9 g (34%) of title compound as a white solid, m.p. 101°-104° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05273993
출처 데이터셋uspto-grants-1993_12
ORD IDord-048e6a4b72cd49d3beac00ce2e218e29
출처 메모uspto-grants-1993_12