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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650472Generated: October 26, 2026

Benzyl Bromide → Methyl 3-(benzyloxy)benzoate

https://huagongshe.com/reaction/650472

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) d 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 numberUS06274336B1
Source datasetuspto-grants-2001_08
ORD IDord-e5c54abfdd4d4a7f976aade4f26de904
Source noteuspto-grants-2001_08