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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 487207생성일: 2026년 10월 25일

Hydrochloric Acid → Methyl 6-Fluoro-3,4-dihydro-4-(methoxycarbonyl)-2H-benzopyran-4-butanoate

https://huagongshe.com/reaction/487207

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물Methyl 4-bromobutyrateHCID 107604—
반응물Methyl 6-fluorochromane-4-carboxylateHCID 14986536—
용매DimethylformamideHCID 6228—
생성물Methyl 6-Fluoro-3,4-dihydro-4-(methoxycarbonyl)-2H-benzopyran-4-butanoateHCID 19094438—

반응 단계

To a suspension of 8.81 g (0.183 mol) 50% NaH in 300 ml of DMF was added, dropwise, a solution of 27.5 g (0.131 mol) of methyl 6-fluoro-2,3-dihydro-4H-benzopyran-4-carboxylate in 100 ml of DMF. After stirring at room temperature for 1 hour, a solution of 33 g (0.183 mol) of methyl 4-bromobutyrate in 25 ml of DMF was added. The resultant homogeneous solution was stirred at room temperature for 16 hours and then poured onto ice/H2O and acidified to pH 3.0 with concentrated HCl. The aqueous was extracted twice with CH2Cl2 and the combined extracts were dried (NaSO4) and filtered. The filtrate was evaporated in vacuo to an oil (44 g) which was purified by column chromatography on 2 Kg of silica gel, eluting with CH2Cl2 /Et2O.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05294635
출처 데이터셋uspto-grants-1994_03
ORD IDord-96d56e5148254c74b3bf53735d2b1973
출처 메모uspto-grants-1994_03