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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107059Generated: October 31, 2026

4-Chloro-N-(1,1-dimethyl-2-propynyl)benzamide → 2-(4-Chlorophenyl)-4,5-dihydro-4,4-dimethyl-5-methyleneoxazole

https://huagongshe.com/reaction/1107059

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-N-(1,1-dimethyl-2-propynyl)benzamideHCID 32738—
CatalystCuprous chlorideHCID 62652—
SolventButyl AcetateHCID 31272—
Product2-(4-Chlorophenyl)-4,5-dihydro-4,4-dimethyl-5-methyleneoxazoleHCID 10867855100.2%

Reaction Conditions

Temperature95 °C

Reaction Steps

A round bottom flask was charged with N-(3-methylbutyn-3-yl)-4-chlorobenzamide (4.5 g, 19.09 mmol), copper(I) chloride (9.5 mg, 0.5 mol %), and n-butyl acetate (20 mL). The resulting mixture was heated to 95° C. for 4 h, then cooled to room temperature. The reaction was washed with 1 M hydrochloric acid solution and with water. The organic layer was dried over anhydrous sodium sulfate. The solvent was removed by evaporation under reduced pressure, and the residue was dried in a vacuum oven to afford 2-(4-chlorophenyl)-4,4-dimethyl-5-methyleneoxazoline (4.24 g, 94% yield) as a pale yellow oil (bp 95° C., 0.6 mm Hg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057477
Source datasetuspto-grants-2000_05
ORD IDord-c58de19889f94a969e34a18c6c4e3933
Source noteuspto-grants-2000_05