Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49701Generated: October 29, 2026

Ethanol → 2-(2-(O-tolylamino)benzo[d]oxazol-6-yl)acetic acid

https://huagongshe.com/reaction/49701

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-Methylphenyl isothiocyanateHCID 69195—
Reactant(3RS)-3-{5-[2-(4-Methyl-2-o-tolylamino-benzoxazol-6-yl)acetylamino]pyrid-2-yl}butyric acidHCID 9955805—
Product2-(2-(O-tolylamino)benzo[d]oxazol-6-yl)acetic acidHCID 23508315—

Reaction Steps

A mixture of ethyl 4-amino-3-hydroxy-phenylacetate (3.3 g, Reference Example 3) and o-tolylisothiocyanate (2.5 mL) in ethanol (150 mL) was stirred at room temperature for about 2 hours. After standing at room temperature overnight the mixture was evaporated and the residue was subjected to flash chromatography on silica eluting with a mixture of pentane and ethyl acetate (7:3, v/v) to give a yellow foam. A solution of this material in ethanol (150 mL) was treated with dicyclohexylcarbodiimide (3.0 g) and the mixture was heated at reflux temperature for 2 hours. The mixture was evaporated and the residue subjected to short column chromatography on silica eluting with a mixture of 5-10% tert-butyl methyl ether in dichloromethane to remove dicyclohexylurea. The resulting light yellow oil was dissolved in ethanol (100 mL) and the solution was treated with sodium hydroxide solution (15 mL, 1M) then heated at reflux temperature for 2 hours. The reaction mixture was evaporated and the residue was dissolved in water. The solution was washed with ethyl acetate and the aqueous layer was acidified to pH 1 by addition of concentrated hydrochloric acid. The resulting white precipitate was collected by filtration, then washed thoroughly with water, and then dried to give the title compound (1.8 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706738B2
Source datasetuspto-grants-2004_03
ORD IDord-77ad59374b41438bb0b895c7dd2b255d
Source noteuspto-grants-2004_03