돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 69473생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/69473

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 at −78° C. to a solution of diisopropylamine (33.5 mL) in dry THF (190 mL). Then the reaction mixture was warmed to room temperature for 5 min, and then cooled again 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. Then the reaction mixture was allowed to return to room temperature and it was stirred at this temperature for 4 h. Water was added to the reaction mixture, then the THF was removed in vacuum and then the aqueous phase was extracted with diethyl ether. The aqueous phase was acidified with conc. HCl, the precipitate obtained was filtered off and washed with water several times. In this way the product was obtained with molecular weight 178.06 (C10H10O3); MS (ESI): 179 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822495B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-7fc365ab56c64ed2a4187612a70af1c8
출처 메모uspto-grants-2014_09