Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918686Generated: October 30, 2026

Ethanol → Ethyl 3-benzylamino-5-sulphamyl-4-(beta,beta, beta-trifluoroethoxy)-benzoate

https://huagongshe.com/reaction/918686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantBenzyl BromideHCID 7498—
Reactant3-Amino-5-sulphamyl-4-(beta,beta,beta-trifluoroethoxy)-benzoic acidHCID 21506001—
ProductEthyl 3-benzylamino-5-sulphamyl-4-(beta,beta, beta-trifluoroethoxy)-benzoateHCID 21505983—

Reaction Steps

A mixture of 3-amino-5-sulphamyl-4-(β, β, β-trifluoroethoxy)-benzoic acid (0.6 g), benzyl bromide (1.2 g), and dry ethanol (8 ml) was refluxed for 5 hours. After cooling, the precipitated ethyl 3-benzylamino-5-sulphamyl-4-(β, β, β-trifluoroethoxy)-benzoate was collected by suction and recrystallized from dry ethanol. After drying, the compound had a melting point of 163-165°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03971819
Source datasetuspto-grants-1976_07
ORD IDord-a62ca07907e445099d9446cee06bad31
Source noteuspto-grants-1976_07