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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258972Generated: November 2, 2026

Allyl bromide → 2-allyloxy-5-bromobenzoic acid

https://huagongshe.com/reaction/1258972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 5-bromosalicylateHCID 77683—
SolventMethyl Ethyl KetoneHCID 6569—
Product2-allyloxy-5-bromobenzoic acidHCID 8707165—

Reaction Steps

The reaction of methyl 5-bromo-2-hydroxyl-benzoate and allyl bromide in 2-butanone in the presence of potassium carbonate was performed as described in Example 2 to give 2-Allyloxy-5-bromo-benzoic acid as white powder. 1H-NMR (400 MHz, d6-DMSO): 12.98 (s, —CO2H); 7.73 (m, larom. H); 7.62 (m, 1 arom. H); 7.07 (m, 1 arom. H); 5.99 (m, —CH═CH2); 5.47, 5.25 (2 d-like, CH═CH2); 4.62 (d-like, CH2—CH═CH2). 13C-NMR (100 MHz, d6-DMSO): 165.99 (C═O); 156.10; 135.10; 133.00; 132.65; 123.86; 117.15; 116.12; 111.34; 68.84.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466199B2
Source datasetuspto-grants-2013_06
ORD IDord-853f64fa9a674efa94f4be5a0d500446
Source noteuspto-grants-2013_06