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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72804생성일: 2026년 10월 24일

Methanethiol → (tert-Butoxycarbonylimino-thiomorpholin-4-yl-methyl)-carbamic acid tert-butyl ester

https://huagongshe.com/ko/reaction/72804

반응식

참여 물질

역할이름HCID투입량
반응물MethanethiolHCID 878—
반응물TriethylamineHCID 8471—
반응물ThiomorpholineHCID 67164—
반응물1,3-DI-Boc-2-methylisothioureaHCID 546603—
촉매Mercurous ChlorideHCID 24182—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물(tert-Butoxycarbonylimino-thiomorpholin-4-yl-methyl)-carbamic acid tert-butyl esterHCID 67369775—

반응 단계

A solution of [[[(1,1-dimethylethoxy)carbonyl]amino]-(methylthio)methylene]-carbamic acid, 1,1-dimethylethyl ester [CAS 107819-90-9] (21 g, 0.0723 mol) in DMF (450 mL) was treated sequentially with thiomorpholine (7 mL, 0.0723 mol), mercury chloride (19.6 g, 0.0723 mol), and Et3N (30 mL, 0.22 mol) and the reaction mixture was stirred for 18 h. The mixture was diluted with EtOAc and filtered through a pad of diatomaceous earth. The filtrate was concentrated, diluted with water and EtOAc and filtered again through a pad of diatomaceous earth. The filtrate aqueous layer was separated and extracted with EtOAc (2×). The combined organic layers were washed with water, then satd. aq. NaCl, dried, and concentrated. The solid was triturated with 20% Et2O/40-60° C. petrol. The solid was filtered off and was washed with 20% Et2O/40-60° C. petrol followed by 40-60° C. petrol. The solid was dried under vacuum to give 21.2 g (85%) as a white solid. Note: The reaction was performed with a trap for gaseous loss of methanethiol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829011B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-ecb393ba31374a78a579de07f0e712fd
출처 메모uspto-grants-2014_09