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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638217Generated: October 31, 2026

Ethanol → 3-Bromo-4-ethoxybut-3-EN-2-one

https://huagongshe.com/reaction/638217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant3-Buten-2-one, 3-bromo-4-hydroxy-HCID 57358789—
SolventTolueneHCID 1140—
Product3-Bromo-4-ethoxybut-3-EN-2-oneHCID 53423743100%

Reaction Steps

A mixture of 400 ml absolute ethanol and 60 ml toluene was heated to reflux and 20 ml of azeotrope was removed via a Dean Stark trap. To the ethanoltoluene solution was added 33.0 g (0.2 mole) of 3-bromo-4-hydroxy-3-buten-2-one and reflux was continued for 2 hours during which period three aliquots of 20 ml of ethanol-toluene were removed via the trap. The solution was concentrated in vacuo to give 38.6 g (100%) of 3-bromo-4-ethoxy-3-buten-2-one as a mobile oil. 1H-NMR(DMSO-d6)ppm(delta): 8.21 (s, 1H), 4.23 (q, 2H), 2.33 (s, 3H), 1.31 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04560690
Source datasetuspto-grants-1985_12
ORD IDord-daff9c9de03a4b40bb18d28d82446518
Source noteuspto-grants-1985_12