Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372659Generated: November 1, 2026

2-Chlorobenzoxazole → Ethyl (4-(2-benzoxazolyl)amino-3-chlorophenyl)acetate

https://huagongshe.com/reaction/1372659

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzoxazoleHCID 11986—
Reactant(4-Amino-3-chloro-phenyl)-acetic acid ethyl esterHCID 17859298—
SolventChloroformHCID 6212—
SolventO-XyleneHCID 7237—
ProductEthyl (4-(2-benzoxazolyl)amino-3-chlorophenyl)acetateHCID 4460681479%

Reaction Steps

In xylene (10 ml), 2-chlorobenzoxazole (743 μl, 6.51 mmol) and ethyl 4-amino-3-chlorophenylacetate (1.30 g, 6.51 mmol) were heated under reflux for 2 hours. After cooling to room temperature, the reaction mixture was diluted with chloroform (50 ml). The mixture was washed with water, dried over anhydrous sodium sulfate, and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from n-hexane/ethyl acetate (9:1, v/v) eluate fractions, ethyl (4-(2-benzoxazolyl)amino-3-chlorophenyl)acetate (1.70 g, 79%) was obtained as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-9cb8f9a21db647699b4be73efd627eb1
Source noteuspto-grants-2007_01