Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411277Generated: October 27, 2026

Tetrahydrofuran → Ethyl n-carbobenzoxy-4-amino-3,5-dimethylbenzoate

https://huagongshe.com/reaction/411277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium hydrideHCID 24758—
ReactantBenzoic acid, 4-amino-3,5-dimethyl-, ethyl esterHCID 201013—
SolventWaterHCID 962—
ProductEthyl n-carbobenzoxy-4-amino-3,5-dimethylbenzoateHCID 10639914—

Reaction Steps

Ethyl 4-amino-3,5-dimethylbenzoate (2.0 g) was added to a tetrahydrofuran (THF) suspension of sodium hydride (0.82 g) in a nitrogen atmosphere and the mixture was stirred at room temperature for 30 min. Subsequently, carbobenzoxychloride (4.4 ml) was added to the suspension and the mixture was stirred overnight. A small amount of water was added to the reaction solution and the mixture was poured into ice water, followed by extraction with ethyl acetate. Following washing and drying (with magnesium sulfate), the solvent was distilled off under vacuum. The resulting crystal was recovered by filtration in the presence of ethanol and dried under vacuum to yield the end product (3.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559149B1
Source datasetuspto-grants-2003_05
ORD IDord-313c6e3d1c8e4c9794916d90bc6432b6
Source noteuspto-grants-2003_05