HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614379Generated: October 30, 2026
Formamidine acetate → 5-Chloropyrimidine-4-carboxylic acid
https://huagongshe.com/reaction/614379
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formamidine acetate | HCID 160693 | — |
| Reactant | Mucochloric Acid | HCID 2771871 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Chloropyrimidine-4-carboxylic acid | HCID 20029396 | 35.1% |
Reaction Steps
Sodium methoxide (162 g) is added to a solution of mucochloric acid (169 g) and formamidine acetate (208 g) in methanol (3 liters) over the course of 20 minutes, and the reaction mixture is heated for 1 hour at 35°-40° C., and then for one and a half hours under reflux. The solvent is removed and water (500 cc) is added to the residue. The aqueous mixture is extracted with ethyl acetate (2 liters). The aqueous phase is brought to pH 1 by the addition of concentrated hydrochloric acid, and the aqueous phase is extracted with ethyl acetate (5 liters). The organic phase is dried over anhydrous magnesium sulphate, filtered and then concentrated to dryness. The residue is washed with diethyl ether (300 cc) and then with diisopropyl ether (600 cc). 4-Carboxy-5-chloropyrimidine (55.6 g), melting at 190° C., is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04144339 |
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| Source dataset | uspto-grants-1979_03 |
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| ORD ID | ord-3a46c32cb00c48b088a319e662afffb7 |
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| Source note | uspto-grants-1979_03 |
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