HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563894Generated: October 31, 2026
Phosphorus oxychloride → 4-Chloro-2-(trifluoromethyl)pyrimidine
https://huagongshe.com/reaction/563894
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178516506 | HCID 178516506 | — |
| Product | 4-Chloro-2-(trifluoromethyl)pyrimidine | HCID 15294369 | — |
Reaction Steps
To 2-(trifluoromethyl)pyrimidin-4-ol (2 g, 12 mmol) was added POCl3 (15 mL). It was refluxed overnight. The solvent was removed. 1N NaOH was added to the reaction mixture slowly until pH=10. The mixture was extracted with DCM (3×80 mL). Combined DCM layer dried over Na2SO4 and taken to dryness. The crude product was vacuum distilled. 4-chloro-2(trifluromethyl)pyrimidine was obtained as a clear oil. (94%). 1H NMR (400 MHz, DCM) δ: 7.60 (d, J=3 Hz, 1H), 8.80 (d, J=3 Hz, 1H), To a mixture of compound 30a (137 mg, 0.75 mmol) and compound 4b (235 mg, 0.75 mmol) in IPA (1 mL), was added TEA (210 mL, 1.5 mmol). The reaction was heated in microwave oven at 140° C. for 20 min. HPLC yielded the desired product as a white powder (28 mg, 6.4%). 1H NMR (400 MHz, DMSO) δ: 1.04 (m, 2 H), 1.62 (m, 6 H), 1.88 (m, 1 H), 2.73 (m,1 H), 4.34 (m, 2 H), 7.09-7.37 (m, 6 H), 8.41 (s, 1 H). Anal. (C22H22N7OF3.0.52TFA.0.54H2O) C, H, N. APCI-MS:[M+H] 458.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08067591B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-5299c18f9ed0457e8a0263ed6e07be6e |
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| Source note | uspto-grants-2011_11 |
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