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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1913482생성일: 2026년 10월 25일

Formaldehyde → 1-(2,3-Dihydro-1,4-benzodioxin-6-yl)-3-(dimethylamino)propan-1-one

https://huagongshe.com/reaction/1913482

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Dimethylamine, hydrochlorideHCID 10473—
반응물1,4-Benzodioxan-6-yl methyl ketoneHCID 76143—
촉매Hydrochloric AcidHCID 313—
용매EthanolHCID 702—
생성물1-(2,3-Dihydro-1,4-benzodioxin-6-yl)-3-(dimethylamino)propan-1-oneHCID 282501882%

반응 단계

A solution of 1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)ethanone (XV) (11 mmol), dimethylamine hydrochloride (14 mmol), paraformaldehyde (16 mmol) and 12 N HCl (2 drops) in ethanol (5 mL) was refluxed overnight. The solution was cooled to room temperature and the ethanol was evaporated under vacuum. The residue was treated with ethyl acetate, heated slightly and sonicated to disperse into fine particles. The solids were filtered and dried at room temperature to produce 1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-3-(dimethylamino)propan-1-one (XVI) as a white solid, (82% yield), 1H NMR (CDCl3, 400 MHz): δ ppm 2.77 (s, 6H), 3.41 (m, 2H), 3.56 (m, 2H), 4.25 (m, 4H), 6.85 (m, 1H), 7.45 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08609717B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-4349373024974d779f9d75d81ecb11a8
출처 메모uspto-grants-2013_12