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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182790Generated: November 3, 2026

Benzyl Bromide → Methyl 4-benzyloxy-2-hydroxy-5-isopropylbenzoate

https://huagongshe.com/reaction/1182790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2,4-dihydroxy-5-(propan-2-yl)benzoateHCID 59167875—
SolventAcetonitrileHCID 6342—
ProductMethyl 4-benzyloxy-2-hydroxy-5-isopropylbenzoateHCID 5823645283.2%

Reaction Steps

A mixture of methyl 2,4-dihydroxy-5-isopropylbenzoate (1.05 g, 5.0 mmol) and anhydrous potassium carbonate (828 mg, 6.0 mmol) in acetonitrile (25 ml) was treated with benzyl bromide (0.655 ml, 5.5 mmol) and the mixture was stirred at room temperature for 24 hours. The solvent was removed in vacuo and the residue was treated with water (50 ml). The solid material was collected by suction filtration, rinsed with water (2×50 ml) and sucked dry under reduced pressure to afford methyl 4-benzyloxy-2-hydroxy-5-isopropylbenzoate (1.25 g, 83%) as colourless needles. 1H NMR (DMSO-d6) 10.68 (1H, br s), 7.57 (1H, s), 7.48-7.40 (4H, m), 7.34 (1H, m), 6.64 (1H, s), 5.20 (2H, s), 3.87 (3H, s), 3.18 (1H, m), 1.17 (6H, d). MS: [M+H]+ 301.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664218B2
Source datasetuspto-grants-2014_03
ORD IDord-e6e5fa1ab25846eab705e22d3c7d3c3c
Source noteuspto-grants-2014_03