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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643828Generated: November 1, 2026

Water → Dimethyl 5-(allyloxy)isophthalate

https://huagongshe.com/reaction/1643828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAllyl bromideHCID 7841—
ReactantCesium carbonateHCID 10796—
Reactant1,3-Benzenedicarboxylic acid, 5-hydroxy-, 1,3-dimethyl esterHCID 83065—
SolventDimethylformamideHCID 6228—
ProductDimethyl 5-(allyloxy)isophthalateHCID 10933919100.8%

Reaction Steps

To a mixture of dimethyl 5-hydroxy-isophthalate (10 g, 47.577 mmol), Cs2CO3 (31 g, 95.2mmol) in DMF was added allyl bromide (4.83 mL, 57.1 mmol) drop-wise. After stirring the mixture for 14 hours, the reaction was treated with water, extracted with EtOAc (2×). The combined organic extract was dried over sodium sulfate, filtered and evaporated to provide the desired product as white solid (12 g, 100% yield). The crude product was used without further purification. 1H NMR (300 MHz, CHLOROFORM-d) δ ppm 3.94 (s, 6 H) 4.56-4.71 (m, 2 H) 5.33 (dd, J=10.46, 1.41 Hz, 1 H) 5.39-5.53 (m, 1 H) 5.96-6.17 (m, 1 H) 7.76 (d, J=1.32 Hz, 2 H) 8.28 (t, J=1.41 Hz, 1 H); LC-MS: (ESI)+m/z=251.00 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119624B2
Source datasetuspto-grants-2012_02
ORD IDord-422268dbb6884f42a7d1013244ddaba1
Source noteuspto-grants-2012_02