HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271195Generated: October 25, 2026
2-Chlorobenzyl chloride → N-acetyl-N-(2-chlorobenzyl)-2-phenoxyaniline
https://huagongshe.com/reaction/2271195
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chlorobenzyl chloride | HCID 11906 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Phenoxyacetanilide | HCID 897080 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-acetyl-N-(2-chlorobenzyl)-2-phenoxyaniline | HCID 18407206 | 94.3% |
Reaction Steps
To a suspension of 400 mg of sodium hydride (60% in oil) in 30 ml of dimethylformamide was added 2.00 g of N-acetyl-2-phenoxyaniline at room temperature, followed by stirring at room temperature for 30 minutes. To the solution was added dropwise 1.64 g of 2-chlorobenzyl chloride at room temperature with stirring, followed by stirring for 30 minutes. After addition of ice-water, the reaction mixture was extracted with ether. The extract was washed with 0.5 N hydrochloric acid, a saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium chloride solution, successively, and dried over anhydrous sodium sulfate. After removal of the drying agent by filtration, the solvent was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent; ethyl acetate-hexane=1:4) to give 2.92 g of N-acetyl-N-(2-chlorobenzyl)-2-phenoxyaniline as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06333358B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-157b8ec5bb6f4d62828b88481518bae7 |
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| Source note | uspto-grants-2001_12 |
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