HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378400Generated: October 25, 2026
Triethylamine → 4-Chloro-5-methoxy-6-(methoxymethyl)pyrimidine
https://huagongshe.com/reaction/1378400
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178494688 | HCID 178494688 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 4-Chloro-5-methoxy-6-(methoxymethyl)pyrimidine | HCID 15279350 | — |
Reaction Steps
85.0 g (0.5 mol) of 4-hydroxy-5-methoxy-6-methoxymethylpyrimidine were suspended in 600 ml of dichloroethane, 50.5 g of triethylamine were added, and 260 g (1.7 mol) of phosphorus oxychloride were then added without cooling. The mixture was stirred for 3 hours at 80° C., poured into ice-water and neutralized by adding solid sodium carbonate, the organic phase was separated, and the water phase was extracted several times by stirring with methylene chloride. The combined organic phases were dried and concentrated. The residue was distilled under a water pump vacuum. 66.1 g (70% of theory) of a yellow oil were obtained. B.p. 93°-96° C./0.1mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05668140 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-3d4eae15b48d410c83b87577a98525b3 |
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| Source note | uspto-grants-1997_09 |
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