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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580950Generated: October 27, 2026

Allyl bromide → Ethyl 3-{4-[(prop-2-en-1-yl)oxy]phenyl}propanoate

https://huagongshe.com/reaction/580950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4-hydroxyhydrocinnamateHCID 2736435—
SolventMethyl Ethyl KetoneHCID 6569—
ProductEthyl 3-{4-[(prop-2-en-1-yl)oxy]phenyl}propanoateHCID 1934897197.2%

Reaction Steps

Allyl bromide (2.30 g) was added to a stirred suspension of ethyl 3-(4-hydroxyphenyl)propionate (3.49 g) and anhydrous potassium carbonate (2.76 g) in butan-2-one (30 ml). The reaction mixture was heated at reflux for 18 hours. The reaction mixture was allowed to cool to ambient temperature and the mixture was filtered. The filtrate was evaporated to give an oil which was purified by column chromatography on silica gel (Merck.Art. No. 9385) using a 4:1 (v/v) mixture of n-hexane and ethyl acetate as eluent to give ethyl 3-(4-allyloxyphenyl)propionate (4.09 g) as a colourless oil; NMR (CDCl3): 1.22 (3H, t), 2.48 (2H, t), 2.88 (2H, t), 4.13 (2H, q), 4.51 (2H, m), 5.25-5.42 (2H, m), 5.95-6.15 (1H, m), 6.83 (2H, d) and 7.03 (2H, d); m/z 235 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05919793
Source datasetuspto-grants-1999_07
ORD IDord-5a2bdee2237346168fe2f46f62cd61b0
Source noteuspto-grants-1999_07