HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271191Generated: October 30, 2026
Water → N-acetyl-N-(2-isopropoxybenzyl)-2-phenoxyaniline
https://huagongshe.com/reaction/2271191
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(2-isopropoxybenzyl)-2-phenoxyaniline | HCID 18407213 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-acetyl-N-(2-isopropoxybenzyl)-2-phenoxyaniline | HCID 13005995 | — |
Reaction Steps
In 30 ml of tetrahydrofuran were dissolved 2.65 g of N-(2-isopropoxybenzyl)-2-phenoxyaniline and 1.5 ml of triethylamine, and then 0.8 ml of acetyl chloride was added dropwise to the solution with stirring, followed by stirring for 30 minutes. The reaction mixture was poured to water and extracted with ethyl acetate, and the extract was washed with 0.5 N hydrochloric acid, a saturated aqueous sodium bicarbonate solution and then with a saturated aqueous sodium chloride solution, successively, and dried over anhydrous sodium sulfate. After removal of the drying agent by filtration, the filtrate 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-isopropoxybenzyl)-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-12718e09ac6a4521a786533b26484509 |
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| Source note | uspto-grants-2001_12 |
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