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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389094Generated: October 30, 2026

tert-Butyl carbazate → HCID 58244228, compound

https://huagongshe.com/reaction/389094

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl carbazateHCID 70091—
ReactantHCID 57467471HCID 57467471—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
ProductHCID 58244228HCID 5824422868.6%

Reaction Steps

WSC•monohydrochloride (18.1 g), tert-butyl carbazate (10.5 g) and 4-(dimethylamino)pyridine (461 mg) were sequentially added to a solution of 2-(4-chloro-2-fluorophenoxy)-2-methylpropanoic acid (17.6 g) in acetonitrile (170 ml), followed by stirring at room temperature for 14 hours. The reaction solution was concentrated under reduced pressure and ethyl acetate was then added thereto. The organic layer was washed with water, 0.5M hydrochloric acid, saturated aqueous sodium bicarbonate solution-water (1:1) and then saturated brine in this order and was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure. The resulting oil (21.8 g) was dissolved in ethyl acetate, 4M hydrogen chloride-ethyl acetate was added thereto, followed by stirring at room temperature for 5 hours and was then concentrated under reduced pressure. Ethyl acetate was added thereto, followed by stirring and the solid was thus separated by filtration. Saturated aqueous sodium bicarbonate was added to the solid thus obtained, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine-water (1:1) and then saturated brine in this order and was dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure to obtain, as a colorless oil, 2-(4-chloro-2-fluorophenoxy)-2-methylpropanohydrazide (12.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377923B2
Source datasetuspto-grants-2013_02
ORD IDord-f564b47362ba4458be046d7e263a6a27
Source noteuspto-grants-2013_02