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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1410274Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1410274

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktDimethylamine, hydrochlorideHCID 10473—
Edukt1,4-Benzodioxan-6-yl methyl ketoneHCID 76143—
KatalysatorHydrochloric AcidHCID 313—
LösungsmittelEthanolHCID 702—
Produkt1-(2,3-Dihydro-1,4-benzodioxin-6-yl)-3-(dimethylamino)propan-1-oneHCID 282501882%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08921413B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-a49a61ad0a894e098379c8482865edc3
Quellennotizuspto-grants-2014_12