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HRID 16357생성일: 2026년 10월 24일

Imidazole → tert-butyl [(1R,2R)-2-(tert-butyldiphenylsilanyloxy)-1-(3,4,5-trifluorophenyl)propyl]carbamate

https://huagongshe.com/ko/reaction/16357

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물DimethylformamideHCID 6228—
반응물tert-ButyldiphenylchlorosilaneHCID 94078—
반응물tert-butyl [(1R,2R)-2-hydroxy-1-(3,4,5-trifluorophenyl)propyl]carbamateHCID 68717986—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물tert-butyl [(1R,2R)-2-(tert-butyldiphenylsilanyloxy)-1-(3,4,5-trifluorophenyl)propyl]carbamateHCID 68718850—

반응 단계

In nitrogen atmosphere, tert-butyldiphenylsilyl chloride (2.0 mL) was added dividedly four times to a DMF solution (3 mL) of [(1R,2R)-2-hydroxy-1-(3,4,5-trifluorophenyl)-propyl]carbamic acid tert-butyl ester (610 mg) and imidazole (817 mg). The resulting reaction solution was stirred at room temperature for 3 hr, and ethyl acetate and water were added thereto. The organic layer was separated and washed with 1 N hydrochloric acid, water, a saturated sodium hydrogencarbonate aqueous solution, and saturated saline in this order. Then, the organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:diethyleter=49:1 to 19:1) to give 684 mg of the title compound. The physical property values of this compound were as follows:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737141B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-33dcc2959eb240baaf16901c524efb4b
출처 메모uspto-grants-2010_06