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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1704464생성일: 2026년 10월 25일

Triethylamine → 5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonate

https://huagongshe.com/reaction/1704464

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-oneHCID 3017358—
용매DichloromethaneHCID 6344—
생성물5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonateHCID 8673535953%

반응 단계

To a stirred and cooled (ice-water bath) mixture of 14.1 parts of 5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one, 8 parts of N,N-diethylethanamine and 195 parts of dichloromethane are added dropwise 7.8 parts of methanesulfonyl chloride. Upon completion, stirring is continued first for 15 minutes while still cooling an further for 1 hour at reflux temperature. The dichloromethane is evaporated and the residue is dissolved in 4-methyl-2-pentanone and water while heating. The layers are separated and the organic phase is stirred with 100 parts of water, while cooling in an ice-bath. The precipitated product is filtered off and dried, yielding 10 parts (53%) of 5-chloro-1,3-dihydro-1-(3-hydroxypropyl)-2H-benzimidazol-2-one methanesulfonate; mp. 140° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04126687
출처 데이터셋uspto-grants-1978_11
ORD IDord-502e2b96607a4e4fa642f3e11b310819
출처 메모uspto-grants-1978_11