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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107071Generated: October 31, 2026

Benzyl Bromide → Methyl 3-(benzyloxy)benzoate

https://huagongshe.com/reaction/1107071

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-746036b479ed49e5b2cdd40684cd3d93
Source noteuspto-grants-2000_05