HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084632Generated: October 31, 2026
Phenylacetyl chloride → N-(3-chloro-alpha,alpha-dimethylbenzyl)-N-(2-oxopropyl)phenylacetamide
https://huagongshe.com/reaction/1084632
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(3-Chloro-alpha,alpha-dimethylbenzylamino)-2-propanone | HCID 15754157 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N-(3-chloro-alpha,alpha-dimethylbenzyl)-N-(2-oxopropyl)phenylacetamide | HCID 15754160 | 62.5% |
Reaction Steps
22.6 g (0.1 mol) of 1-(3-chloro-α,α-dimethylbenzylamino)-2-propanone prepared by the method of Reference Example 5, was dissolved in 200 ml of acetone, and 14.0 g (0.11 mol) of potassium carbonate was added thereto. The mixture was cooled with ice water, and then 15.5 g (0.1 mol) of phenylacetyl chloride was gradually dropwise added thereto under stirring. After completion of the dropwise addition, the reaction mixture was returned to room temperature and stirred for 3 hours. Then, the solvent was distilled off under reduced pressure, and then water was added to the residue, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was crystallized from n-hexane to obtain 21.5 g (yield: 62.5%) of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05006157 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-c7472bb6326b4737ba4f023dbaaba528 |
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| Source note | uspto-grants-1991_04 |
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