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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Thiophene, 2,4-dibromo- | HCID 2724560 | — |
| 반응물 | 3,3a,4,5-tetrahydro-7H-pyrano[3,4-c]isoxazole | HCID 57475675 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran toluene | HCID 22635083 | — |
| 생성물 | (+/-)-(3aR*,7aS*)-7a-(4-bromothiophen-2-yl)-hexahydropyrano[3,4-c]isoxazole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08198269B2 |
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| 출처 데이터셋 | uspto-grants-2012_06 |
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| ORD ID | ord-890d4fed85954240810fff31d0d6b694 |
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| 출처 메모 | uspto-grants-2012_06 |
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