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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1887545생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1887545

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물DiisopropylamineHCID 7912—
반응물4-Methoxy-2-methylbenzoic acidHCID 597216—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물6-Methoxy-3,4-dihydro-1H-2-benzopyran-1-oneHCID 12401182—

반응 단계

A 1.6M solution of n-butyllithium in hexane (145.9 mL) was added dropwise to a solution of diisopropylamine (33.5 mL) in dry THF (190 mL) at −78° C. The reaction mixture was then warmed to room temperature for 5 min and again cooled to −78° C., and a solution of 4-methoxy-2-methylbenzoic acid in dry THF (210 mL) was added dropwise. After stirring at this temperature for 10 min, paraformaldehyde (7 g) was added. The reaction mixture was then allowed to reach room temperature and was stirred at this temperature for 4 h. Water was added to the reaction mixture, and then the THF was removed in vacuo and 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 with water several times. The product with the molecular weight of 178.06 (C10H10O3) was obtained in this way; MS (ESI): 179 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08501771B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-e15a35bf3666477b9f2686c170eaecf4
출처 메모uspto-grants-2013_08