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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453794Generated: October 31, 2026

Pyridine → N-(5-tert-Butyl-1,2-oxazol-3-yl)-2-chloroacetamide

https://huagongshe.com/reaction/1453794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChloroacetyl chlorideHCID 6577—
Reactant3-Isoxazolamine, 5-(1,1-dimethylethyl)-HCID 171473—
SolventDichloromethaneHCID 6344—
ProductN-(5-tert-Butyl-1,2-oxazol-3-yl)-2-chloroacetamideHCID 28065541132.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

Chloroacetic acid chloride (0.93 ml; II.42 mmol) is dropped slowly into a stirred solution of 5-t-Butyl-3-amino isoxazole (1.5 g; 7.67 mmol) in pyridine (1.09 ml; 13.49 mmol) and dichloromethane (20 ml), cooled to 0° C. Stirring is continued for 2 h at room temperature. The reaction mixture is diluted with dichloromethane, washed twice with 1N aqueous hydrochloric acid, twice with an aqueous solution of NaHCO3 and with water. The reaction mixture is then dried over Na2SO4, filtered and evaporated to yield 2.2 g (98%) brownish solid of 10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476683B2
Source datasetuspto-grants-2009_01
ORD IDord-8f158e65f616455e926b177b9eb292ca
Source noteuspto-grants-2009_01