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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708400Generated: October 30, 2026

Acetamidine monohydrochloride → HCID 178440130, compound

https://huagongshe.com/reaction/1708400

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamidine monohydrochlorideHCID 67170—
ReactantSodiumHCID 5360545—
ReactantHCID 9971622HCID 9971622—
SolventEthanolHCID 702—
ProductHCID 178440130HCID 17844013055.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05358950
Source datasetuspto-grants-1994_10
ORD IDord-d9bc27595328438f96ce9099cb07e0cd
Source noteuspto-grants-1994_10