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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1913833생성일: 2026년 10월 25일

Formaldehyde → 6-Methoxy-3,4-dihydro-1H-2-benzopyran-1-one

https://huagongshe.com/reaction/1913833

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물DiisopropylamineHCID 7912—
반응물4-Methoxy-2-methylbenzoic acidHCID 597216—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물6-Methoxy-3,4-dihydro-1H-2-benzopyran-1-oneHCID 12401182—

반응 단계

To a solution of diisopropylamine (33.5 ml) in dry THF (190 ml) was added dropwise, at −78° C., n-butyllithium (1.6 M solution in hexane, 145.9 ml). Subsequently, the reaction mixture was warmed to room temperature for 5 minutes and then cooled again to −78° C., and a solution of 4-methoxy-2-methylbenzoic acid (10 g) in dry THF (210 ml) was added dropwise. After stirring at this temperature for 10 minutes, paraformaldehyde (7 g) was added. The reaction mixture was then allowed to come to room temperature and stirred at this temperature for 4 hours. The reaction mixture was admixed with water, then the THF was removed under reduced pressure and then the aqueous phase was extracted with diethyl ether. The aqueous phase was acidified with conc. HCl, and the resulting precipitate was filtered off and washed repeatedly with water. The product was thus obtained with the molecular weight of 178.06 (C10H10O3); MS (ESI): 179 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08609731B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-cdb9bb6afbfa437d8f42d7b851829380
출처 메모uspto-grants-2013_12