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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361528Generated: October 30, 2026

o-Xylyl bromide → Methyl 3-hydroxy-5-{[(2-methylphenyl)methyl]oxy}benzoate

https://huagongshe.com/reaction/1361528

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-Xylyl bromideHCID 6992—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 3,5-DihydroxybenzoateHCID 75076—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-hydroxy-5-{[(2-methylphenyl)methyl]oxy}benzoateHCID 2107422729.8%

Reaction Conditions

Temperature15 °C

Reaction Steps

To a solution of methyl 3,5-dihydroxybenzoate (50 g, 0.30 mol) in DMF (500 ml) at 0° C. was added sodium hydride (10.8 g, 0.27 mol) portion wise. The reaction was allowed to warm to 15° C., and stirred for 20 minutes. The mixture was re-cooled to 0° C. and a solution of 2-methylbenzyl bromide (36 ml, 0.27 mol) in DMF (50 ml) was added over 30 minutes. The reaction was warmed to ambient temperature and concentrated in vacuo. The residual oil was partitioned between ethyl acetate (500 ml) and water (250 ml), and the ethyl acetate layer was separated, washed with water and evaporated. The residue was purified by column chromatograph on silica gel (gradient, 0-100% ethyl acetate in isohexane) to give the desired compound (21.9 g, 27%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880012B2
Source datasetuspto-grants-2011_02
ORD IDord-8fd60ed9337946ae96816980a4428be1
Source noteuspto-grants-2011_02