HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708400Generated: October 30, 2026
Acetamidine monohydrochloride → HCID 178440130, compound
https://huagongshe.com/reaction/1708400
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetamidine monohydrochloride | HCID 67170 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 9971622 | HCID 9971622 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178440130 | HCID 178440130 | 55.6% |
Reaction Steps
3.5 g of sodium are dissolved in 175 ml of ethanol. 9.5 g of acetamidine hydrochloride are added to this solution and the mixture is stirred for 5 minutes at room temperature. 20 g of ethyl 2-(4-nitrobenzyl)-3-oxohexanoate, prepared in Example 3, are then added and the mixture is stirred for 4 days at room temperature. The solvents are then evaporated off under vacuum and the residue is taken up with hydrochloric acid solution and extracted with ethyl acetate. The organic phase is dried over magnesium sulphate and then evaporated under vacuum to give an oily residue which crystallises in an acetone/ether mixture. The crystals are drained and dried and give 10.9 g of 6-n-propyl-2-methyl-4-hydroxy-5-(4-nitrobenzyl)pyrimidine in the form of crystals of melting point 200° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05358950 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-d9bc27595328438f96ce9099cb07e0cd |
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| Source note | uspto-grants-1994_10 |
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