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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453409Generated: October 30, 2026

Benzyl Bromide → 4-Benzyloxy-2-ethyl-3-methylbenzoic acid

https://huagongshe.com/reaction/453409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Ethyl-4-hydroxy-3-methylbenzoic acidHCID 22717373—
SolventAcetoneHCID 180—
Product4-Benzyloxy-2-ethyl-3-methylbenzoic acidHCID 66818581—

Reaction Steps

2.10 g of 2-ethyl-4-hydroxy-3-methylbenzoic acid (E1) are dissolved in 50 ml of acetone. 3.30 ml of benzyl bromide and 5.10 g of K2CO3 are subsequently added. The reaction suspension is heated under reflux for 18 h overnight, subsequently filtered off with suction, and the filtrate obtained is evaporated to dryness in vacuo. The residue is dissolved in 40 ml of ethanol, and 40 ml of 2.0 N NaOH solution are added. The mixture is then heated under reflux for 3 h. The clear solution is diluted with 150 ml of water and adjusted to pH 1 using 20% hydrochloric acid. After stirring for 30 min, the precipitate formed is filtered off with suction, rinsed with water and dried at 90° C. in vacuo overnight, giving 2.45 g of the title compound as a beige, amorphous solid having a melting point of 169° C.; MS: 270.0 (M+); TLC: Rf=0.36 (cyclohexane/ethyl acetate 2:1 parts by volume).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492440B2
Source datasetuspto-grants-2013_07
ORD IDord-7c7295df93174aa9aa0c3f9b5fa44091
Source noteuspto-grants-2013_07