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HRID 469900作成日:2026年10月25日

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

https://huagongshe.com/reaction/469900

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物Dimethylamine, hydrochlorideHCID 10473—
反応物1,4-Benzodioxan-6-yl methyl ketoneHCID 76143—
触媒Hydrochloric AcidHCID 313—
溶媒EthanolHCID 702—
生成物1-(2,3-Dihydro-1,4-benzodioxin-6-yl)-3-(dimethylamino)propan-1-oneHCID 282501882%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08629176B1
出典データセットuspto-grants-2014_01
ORD IDord-bf34c636d63443c397514f67538c9206
出典メモuspto-grants-2014_01