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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252223Generated: November 2, 2026

4,6-Dimethyl-2-(4-nitrobenzyloxycarbonylthio)pyrimidine → 3-(p-Nitrobenzyloxycarbonyl)aminomethylbenzyl alcohol

https://huagongshe.com/reaction/1252223

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,6-Dimethyl-2-(4-nitrobenzyloxycarbonylthio)pyrimidineHCID 13504316—
Reactant[3-(Aminomethyl)phenyl]methanolHCID 21880609—
SolventTetrahydrofuranHCID 8028—
Product3-(p-Nitrobenzyloxycarbonyl)aminomethylbenzyl alcoholHCID 54053962—

Reaction Steps

To 3-hydroxymethylbenzylamine (1.37 g) in tetrahydrofuran (30 ml), a solution of S-p-nitrobenzyloxycarbonyl-4,6-dimethyl-2-mercaptopyrimidine (6.2 g) in tetrahydrofuran (20 ml) was added at room temperature, followed by stirring for 1 hours. The resulting precipitates were removed by filtration and the filtrate was diluted with ethyl acetate, washed with water, dried over anhydrous sodium sulfate and evaporated in vacuo to give an oily residue which was then crystallized from diethyl etherdichloromethane to give 3-(p-nitrobenzyloxycarbonyl)aminomethylbenzyl alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04742052
Source datasetuspto-grants-1988_05
ORD IDord-7822ed32ed3a4e20ab8061e3bff0feaf
Source noteuspto-grants-1988_05