HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271214Generated: November 3, 2026
Hexamethylphosphoramide → HCID 18407196, compound
https://huagongshe.com/reaction/2271214
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 18407219 | HCID 18407219 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18407196 | HCID 18407196 | — |
Reaction Steps
In a mixture of 10 ml of tetrahydrofuran and 0.1 ml of hexamethylphosphoramide was dissolved 0.50 g of N-acetyl-N-(2-carboxybenzyl)-2-phenoxyaniline, and 0.2 ml of thionyl chloride was added, followed by stirring at room temperature for 3 hours. The reaction mixture was concentrated, the residue was dissolved in 10 ml of tetrahydrofuran, and 2 ml of 50% aqueous dimethylamine solution was added dropwise with stirring. The reaction mixture was poured into water and extracted with ethyl acetate, and the extract was washed with 1 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=1:3) to give 0.49 g of N-acetyl-N-(2-dimethylaminocarbonylbenzyl)-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-790e6654dea04040808d6baeb0503cab |
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| Source note | uspto-grants-2001_12 |
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