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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 217999생성일: 2026년 10월 27일

Ammonium Chloride → (+/-)-(3aR*,7aS*)-7a-(4-bromothiophen-2-yl)-hexahydropyrano[3,4-c]isoxazole

https://huagongshe.com/reaction/217999

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Thiophene, 2,4-dibromo-HCID 2724560—
반응물3,3a,4,5-tetrahydro-7H-pyrano[3,4-c]isoxazoleHCID 57475675—
반응물ButyllithiumHCID 178418339—
용매Tetrahydrofuran tolueneHCID 22635083—
생성물(+/-)-(3aR*,7aS*)-7a-(4-bromothiophen-2-yl)-hexahydropyrano[3,4-c]isoxazoleHCID 68587825—

반응 단계

n-Butyllithium (2.63 M, 2.99 ml) was added dropwise to a solution of 2,4-dibromothiophene (2.00 g) in toluene-THF (10:1) (22 ml) at −78° C. After stirring at the same temperature for one hour, a solution of (±)-3,3a,4,5-tetrahydro-7H-pyrano[3,4-c]isoxazole obtained in Preparation Example 1-(2) (500 mg) in toluene-THF (10:1) (10 ml) and a boron trifluoride-diethyl ether complex (990 μl) were added dropwise at the same time. After stirring at the same temperature for two hours, an ammonium chloride solution was added to terminate the reaction. The aqueous layer was extracted with ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography to obtain the title compound (700 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198269B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-890d4fed85954240810fff31d0d6b694
출처 메모uspto-grants-2012_06