HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380846Generated: October 31, 2026
Methyl 4-chloroacetoacetate → HCID 178467470, compound
https://huagongshe.com/reaction/1380846
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 4-chloroacetoacetate | HCID 36240 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2-Ethylisouronium chloride | HCID 12298735 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178467470 | HCID 178467470 | — |
Reaction Steps
A mixture of 24.9 g (0.2 mol) of O-ethylisourea hydrochloride and 21.5 g (0.14 mol) of methyl 4-chloroacetoacetate in 100 ml of methanol is treated at 0°-5° C. during 10 minutes with a solution of 7.55 g (0.33 mol) of sodium in 100 ml of methanol. The mixture is stirred at 0° C. for 2 hours and at room temperature for 18 hours and the solvent is then removed by evaporation under reduced pressure. The residue is dissolved in 300 ml of water and the solution is adjusted to a pH-value of 6. The resulting crystallline product is filtered off, washed with diethyl ether and dried at 40° C. In this manner there is obtained 2-ethoxy-4-chloromethyl-6-hydroxy-pyrimidine, m.p. 157°-159° C. By back-extracting the aqueous filtrate three times with 150 ml of chloroform each time there is obtained an additional amount of this product, m.p. 159°-161° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04584295 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-c922cc9b35e54dfa8bc53a909857f975 |
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| Source note | uspto-grants-1986_04 |
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