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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl 4-Hydroxybenzoate | HCID 7180 | — |
| Reactant | Isophthaloyl chloride | HCID 7451 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Di(p-benzyloxycarbonylphenyl)isophthalate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04695649 |
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| Source dataset | uspto-grants-1987_09 |
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| ORD ID | ord-28542f94e7884e4fb773dc42c81f1a9e |
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| Source note | uspto-grants-1987_09 |
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