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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20272Generated: October 29, 2026

Oxalyl chloride → Ammonia

https://huagongshe.com/reaction/20272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactanttert-Butyl carbazateHCID 70091—
Reactant3-(Dimethyl-1,2-oxazol-4-yl)propanoic acidHCID 1092971—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductAmmoniaHCID 222—
Producttert-Butyl 2-[3-(3,5-dimethylisoxazol-4-yl)propanoyl]hydrazinecarboxylateHCID 59347450—

Reaction Steps

Oxalyl chloride (5.16 mL, 59.2 mmol) was added to a solution of β-(3,5-dimethyl-4-isoxazolyl)propionic acid (J. Org. Chem. 59(10); 1994; 2882) (2.5 g, 14.8 mmol) in dichloromethane (50 mL) and N,N-dimethylformamide (1 drop), and the solution was stirred at room temperature for 30 minutes. The mixture was concentrated under reduced pressure and the residue was azeotroped with dichloromethane (5×) to provide a brown liquid. This was dissolved in dichloromethane (25 mL), and tert-butyl carbazate (2.93 g, 22.2 mmol) was added portionwise. The mixture was diluted with further dichloromethane (23 mL) and the reaction was stirred for 18 hours at room temperature. The mixture was concentrated under reduced pressure, the residue was suspended in dichloromethane, the resulting precipitate was filtered off and the filtrate was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using an elution gradient of dichloromethane:methanol:0.88 ammonia (95:5:0.5 to 90:10:1) to provide the title compound as an oil, 3.08 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745630B2
Source datasetuspto-grants-2010_06
ORD IDord-8a2e53c658ff4fa4a615632e52a90fd3
Source noteuspto-grants-2010_06