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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273380Generated: October 25, 2026

Sodium hydride → Methyl 4-[(3-bromophenyl)methoxy]benzenepropanoate

https://huagongshe.com/reaction/273380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant3-Bromobenzyl bromideHCID 69979—
ReactantBenzenepropanoic acid, 4-hydroxy-, methyl esterHCID 79706—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-[(3-bromophenyl)methoxy]benzenepropanoateHCID 23136270144%

Reaction Steps

To a solution of methyl 3-(4-hydroxyphenyl)propanoate (0.3 g, 1.67 mmol) in N,N-dimethylformamide (4.0 mL) was added 60% sodium hydride (0.073 g, 1.83 mmol) at 0° C. with stirring, and the mixture was stirred at the same temperature for 15 min. Then, 3-bromobenzylbromide (0.44 g, 1.75 mmol) was added to the mixture at 0° C. with stirring, and the mixture was stirred at room temperature for 2 hrs. The reaction mixture was diluted with ethyl acetate and washed with 5% aqueous potassium hydrogensulfate solution and saturated brine. The ethyl acetate layer was dried over magnesium sulfate and concentrated under reduced pressure to give the title compound (0.84 g, yield 72%) as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456218B2
Source datasetuspto-grants-2008_11
ORD IDord-1121fc2544844b9485373f654fe62713
Source noteuspto-grants-2008_11