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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852543Generated: October 30, 2026

Benzyl Bromide → Dimethyl 5-bentyloxy-isophthalate

https://huagongshe.com/reaction/852543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-Benzenedicarboxylic acid, 5-hydroxy-, 1,3-dimethyl esterHCID 83065—
SolventAcetoneHCID 180—
ProductDimethyl 5-bentyloxy-isophthalateHCID 7643390105.1%

Reaction Steps

K2CO3 (21 g, 153 mmol, 2 equiv) and benzyl bromide (11 ml, 92 mmol, 1.2 equiv) were added to a solution of 5-hydroxy-isophthalic acid dimethyl ester (D42) (16.1 g, 76.7 mmol, 1 equiv) in acetone (400 ml) at room temperature. The resulting solution was refluxed for 18 h, cooled to room temperature and concentrated in vacuo. The residue was partitioned between H2O and AcOEt. The aqueous phase was extracted with AcOEt and the combined organic layers were washed with 2N aqueous NaOH solution and brine, dried over MgSO4 and concentrated in vacuo to give 5-benzyloxy-isophthalic acid dimethyl ester (D44) (24.2 g, 105%) as a white solid. [M+H]+=301.0, RT=3.50 min

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253198B2
Source datasetuspto-grants-2007_08
ORD IDord-71d980f29f114cd18960011bb8d0f879
Source noteuspto-grants-2007_08