HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606563Generated: October 30, 2026
Phosphorus oxychloride → HCID 22767844, compound
https://huagongshe.com/reaction/1606563
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 21401563 | HCID 21401563 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 22767844 | HCID 22767844 | — |
Reaction Steps
(3-Trifluoromethylphenoxy) (4-chlorophenyl)acetamide, (33.0 g., 0.1 mole) is dissolved in 250 ml. of phosphorus oxychloride and triethylamine (22.2 g.) is added over a 45-minute period with stirring while maintaining the temperature of the solution at 0°-2°C. Over a period of an hour the temperature is allowed to rise to 25°C. and then the solution is heated under reflux for 30 minutes. The solution is concentrated in vacuo (about 200 mm.) to remove volatile products and excess phosphorus oxychloride. Toluene (150 ml.) and ice water (250 ml.) are added to the residue. The toluene layer is separated and the aqueous phase is extracted with 3 × 75 ml. of toluene. The toluene solutions are combined and extracted with 0.5 N sodium hydroxide and then with water. The toluene solvent is removed in vacuo and the residue is distilled in vacuo (0.3 mm.). (3-Trifluoromethylphenoxy) (4-chlorophenyl)acetonitrile (27.6 g.) boiling at 144°-145°C. is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03953465 |
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| Source dataset | uspto-grants-1976_04 |
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| ORD ID | ord-9a527ee6d6894ccc8cca7893d713513e |
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| Source note | uspto-grants-1976_04 |
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