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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132708Generated: October 27, 2026

Catechol → o-Phenylene dibenzoate

https://huagongshe.com/reaction/132708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCatecholHCID 289—
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
ReactantTetrahydrofuranHCID 8028—
SolventWaterHCID 962—
Producto-Phenylene dibenzoateHCID 6951494%

Reaction Steps

To 5.5 g pyrocatechol were added 50 ml tetrahydrofuran and 12.1 ml pyridine with stirring. Then to the resulting homogeneous mixture was slowly added 14.5 ml benzoyl chloride, and the reaction was stirred at room temperature for 1 hour, then heated refluxing for 4 hours. Next, 70 ml water was added to dissolve the resulting salt. The reaction mixture was extracted with toluene. Organic phase was separated, washed with saturated saline for two times, dried over anhydrous sodium sulfate. Removing solvent gave a white solid. After recrystallizing from ethyl acetate, 1,2-phenylene dibenzoate was obtained as a white crystal, the yield was 94%, and m.p. was 75-77° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388061B2
Source datasetuspto-grants-2008_06
ORD IDord-0083c813f29248ca836499c60a0346a2
Source noteuspto-grants-2008_06