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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309561Generated: November 2, 2026

Benzyl 4-Hydroxybenzoate → Di(p-benzyloxycarbonylphenyl)isophthalate

https://huagongshe.com/reaction/2309561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-HydroxybenzoateHCID 7180—
ReactantIsophthaloyl chlorideHCID 7451—
ReactantTriethylamineHCID 8471—
SolventTolueneHCID 1140—
ProductDi(p-benzyloxycarbonylphenyl)isophthalateHCID 13878961—

Reaction Steps

Into a 500 ml four-neck flask equipped with a condenser tube and a thermometer are charged 56 g of benzyl p-hydroxybenzoate, 25 g of triethylamine and 160 ml of toluene. A suspension of 25 g of isophthalic dichloride in 100 ml of toluene is added dropwise with stirring while maintaining the mixture at 0°-3° C. over 3 hours. After addition, the mixture is further allowed to react at 0°-3° C. for 1 hour. Thereafter, the resulting reaction product is collected by filtration to obtain white crystals. The crystalline product is washed with 1500 ml of water twice and then with 1000 ml of methanol twice and subsequently, recrystallized from a mixture solvent of hexane-chloroform (1:1) to give di(p-benzyloxycarbonylphenyl)isophthalate melting at 105°-107° C. as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04695649
Source datasetuspto-grants-1987_09
ORD IDord-28542f94e7884e4fb773dc42c81f1a9e
Source noteuspto-grants-1987_09