HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509002Generated: October 30, 2026
Phosphorus oxychloride → 4-Chloro-6-(3-chlorophenyl)-2-ethylpyrimidine
https://huagongshe.com/reaction/1509002
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 6-(3-Chlorophenyl)-2-ethyl-4(3H)-pyrimidinone | HCID 136509819 | — |
| Product | 4-Chloro-6-(3-chlorophenyl)-2-ethylpyrimidine | HCID 80936219 | 81% |
Reaction Steps
A mixture of 6-(3-chlorophenyl)-2-ethylpyrimidin-4(3H)-one (0.240 g, 1.0 mmol) and POCl3 (5 mL) was heated to 85° C. for 6 h. After this time, the reaction was cooled, neutralized with saturated aqueous sodium bicarbonate, and extracted with methylene chloride. The combined organic layer was dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated. The residue was purified by column chromatography (silica, hexanes/ethyl acetate) to afford the title compound as an off-white solid (0.210 g, 81%). MW=253.13. 1H NMR (CDCl3, 500 MHz) δ 8.10 (t, J=1.9 Hz, 1H), 7.96-7.92 (m, 1H), 7.55-7:41 (m, 3H), 3.03 (q, J=7.6 Hz, 2H), 1.55 (s, 1H), 1.42 (t, J=7.6 Hz, 3H); APCI MS m/z 254 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09221843B2 |
|---|
| Source dataset | uspto-grants-2015_12 |
|---|
| ORD ID | ord-027c68ef52654591b89be018369204f1 |
|---|
| Source note | uspto-grants-2015_12 |
|---|