Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342712Generated: November 1, 2026

Aspirin → HCID 70345089, compound

https://huagongshe.com/reaction/342712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAspirinHCID 2244—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant1,3-Dioxolane-4-methanamine, 2,2-dimethyl-HCID 4122349—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 70345089HCID 70345089—

Reaction Conditions

Temperature0 °C

Reaction Steps

The solution from 2-acetoxybenzoic acid (216 mg, 1.2 mmol) in dichloromethane (4 ml) is treated with triethylamine (0.15 ml, 1.2 mmol), cooled to 0° C., treated dropwise with ethyl chloroformate (0.144 ml, 1.0 mmol), stirred at 0° C. for 2 h and filtered. The filtrate is added at room temperature to a solution of 2,2-dimethyl-4-aminomethyl-1,3-dioxolane (293 mg, 1.0 mmol) and triethylamine (0.14 ml) in dichloromethane (4 ml). After 4 h, water (10 ml) is added and the mixture is stirred. The organic phase is washed with dilute hydrochloric acid, saturated aqueous sodium hydrogencarbonate solution and water, dried over magnesium sulphate and concentrated. The residue is purified by column chromatography on silica gel 60 (gradient hexane/ethyl acetate=3/1→1/1). Yield: 143 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05859053
Source datasetuspto-grants-1999_01
ORD IDord-064ea014797745dd91de2ff86659b7de
Source noteuspto-grants-1999_01