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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258960Generated: October 30, 2026

Allyl bromide → 3-Allyloxy-benzoic acid

https://huagongshe.com/reaction/1258960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3-hydroxybenzoateHCID 24522—
SolventMethyl Ethyl KetoneHCID 6569—
Product3-Allyloxy-benzoic acidHCID 6483884—

Reaction Steps

The reaction of ethyl 3-hydroxybenzoate and allyl bromide in 2-butanone in the presence of potassium carbonate was performed as described in Example 2 to give 3-Allyloxy-benzoic acid as white powder. 1H-NMR (400 MHz, d6-DMSO): 12.97 (s, —CO2H); 7.47 (d-like, 1 arom. H); 7.40 (m, 2 arom. H); 7.18 (m, 1 arom. H); 5.99 (m, —CH═CH2); 5.37, 5.23 (2 d-like, CH═CH2); 4.03 (d-like, CH2—CH_CH2). 13C-NMR (100 MHz, d6-DMSO): 167.08 (C═O); 158.12; 133.44; 132.27; 129.67; 121.66; 119.47; 117.47; 114.78; 68.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466199B2
Source datasetuspto-grants-2013_06
ORD IDord-fd7f734c470c44688f9b2c2b5b191e99
Source noteuspto-grants-2013_06