HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993032Generated: October 30, 2026
Phosphorus oxychloride → 2-(4-Trifluoromethylphenyl)-4-chloromethyl-5-methyloxazole
https://huagongshe.com/reaction/1993032
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Oxazole, 4,5-dimethyl-2-[4-(trifluoromethyl)phenyl]-, 3-oxide | HCID 10515280 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-Trifluoromethylphenyl)-4-chloromethyl-5-methyloxazole | HCID 10236333 | 15% |
Reaction Steps
Phosphorous oxychloride (0.72 mL, 7.8 mmol) was added dropwise to an oven-dried 100 mL pear-shaped flask charged with 18.1 (1.8 g, 7.00 mmol) and dichloromethane (20 mL). The reaction was refluxed under nitrogen atmosphere for 30 minutes and then cooled to room temperature. The reaction was washed with water (2×250 mL) and the combined aqueous layers were back extracted with DCM (2×25 mL). The combined organic layers were washed with brine and dried (Na2SO4). The solvent was removed under reduced pressure and the resulting residue was purified via radial chromatography (15% diethyl ether in hexanes) to yield 216 mg (15%) of 4-chloromethyl-5-methyl-2-(4-trifluoromethyl-phenyl)-oxazole as a white solid. LC/MSD m/e: 276.0 (M+H); 1H NMR (400 MHz) (CDCl3) δ 8.15 (2H, d, J=8.0 Hz), 7.73 (2H. d, J=8.0 Hz), 4.59 (2H, s), 2.48 (2H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07649110B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-4dfc18631b1a46e783a01d1bfe906dae |
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| Source note | uspto-grants-2010_01 |
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