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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 218990생성일: 2026년 10월 25일

Hydrochloric Acid → Carbamic acid, [(2R)-2-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-hydroxyethyl]-, 1,1-dimethylethyl ester

https://huagongshe.com/reaction/218990

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물(R)-2-Methyl-CBS-oxazaborolidineHCID 9838490—
반응물Carbamic acid, [2-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-oxoethyl]-, 1,1-dimethylethyl esterHCID 10870948—
반응물(Dimethyl sulfide)trihydroboronHCID 12423031—
용매TolueneHCID 1140—
용매TetrahydrofuranHCID 8028—
생성물Carbamic acid, [(2R)-2-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-hydroxyethyl]-, 1,1-dimethylethyl esterHCID 1088183885.7%

반응 단계

A 2M solution of borane-dimethyl sulphide in THF (28 ml) was added slowly to a 1M solution of (R)-tetrahydro-1-methyl-3,3-diphenyl-1H,3H-pyrrolo[1,2-c][1,3,2]oxazaborole in toluene (56 ml) at 0° under nitrogen. A solution of tert-butyl 2-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-oxoethylcarbamate, (108.2 g) in THF (1.3 liters) was added slowly keeping the temperature below 5° followed by 2M solution of borane-dimethyl sulphide in THF (252 ml) over 50 min. After 1 h, 2M HCl (170 ml) was added with cooling and the mixture was partitioned between EtOAc and water. The organic layer was washed with saturated NaHCO3 solution and brine and dried (MgSO4). The solution was concentrated and the product purified by chromatography on flash silica gel (800 g), eluting successively with hexane:EtOAc (4:1 then 3:1) to give the title compound (93.3 g), LCMS RT=3.31 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198483B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-7ed40d96b05e4d4587185ba310ea6b8a
출처 메모uspto-grants-2012_06