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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107079Generated: October 30, 2026

Benzyl Bromide → Methyl 3-(benzyloxy)benzoate

https://huagongshe.com/reaction/1107079

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) δ7.67 (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 numberUS06057362
Source datasetuspto-grants-2000_05
ORD IDord-b87f6e91ebee45e29b0f7b9ad9eb2d79
Source noteuspto-grants-2000_05