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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594975Generated: October 30, 2026

Benzyl Bromide → Methyl 3-(benzyloxy)benzoate

https://huagongshe.com/reaction/1594975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 3-HydroxybenzoateHCID 88068—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-(benzyloxy)benzoateHCID 1336803163.8%

Reaction Steps

To a suspension of NaH (0.395 g, 9.87 mmol, 60% in mineral oil) in DMF (20 mL) was added methyl 3-hydroxybenzoate (1.0 g, 6.58 mmol). After stirring for 15 min at room temperature, benzyl bromide (1.1 g, 6.58 mmol) was added. After stirring at room temperature for 3h, the solution was partitioned between ethyl acetate and water. The organic layer was washed with water (2×75 mL), saturated aqueous sodium bicarbonate, and brine, then dried (MgSO4), filtered and concentrated to yield an off-white solid (1.013 g, 4.2 mmol). 1H NMR (400 MHz, CDCl3) δ 7.67 (m, 2H), 7.48-7.34 (m, 6H), 7.19 (m, 1H), 5.12 (s, 2H), 3.95 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06284777B1
Source datasetuspto-grants-2001_09
ORD IDord-f1178043390f41cf82e736ba1a8ffa2e
Source noteuspto-grants-2001_09