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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chloro-N-(1,1-dimethyl-2-propynyl)benzamide | HCID 32738 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | Butyl Acetate | HCID 31272 | — |
| Product | 2-(4-Chlorophenyl)-4,5-dihydro-4,4-dimethyl-5-methyleneoxazole | HCID 10867855 | 100.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06057477 |
|---|
| Source dataset | uspto-grants-2000_05 |
|---|
| ORD ID | ord-c58de19889f94a969e34a18c6c4e3933 |
|---|
| Source note | uspto-grants-2000_05 |
|---|