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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033752Generated: October 30, 2026

Propargyl bromide → 2-(N-Ethoxycarbonyl-N-propargylaminomethyl)-pyrimidine

https://huagongshe.com/reaction/1033752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Ethoxycarbonylaminomethyl-pyrimidineHCID 18953635—
CatalystBenzyltriethylammonium bromideHCID 165294—
SolventTolueneHCID 1140—
Product2-(N-Ethoxycarbonyl-N-propargylaminomethyl)-pyrimidineHCID 18953642—

Reaction Steps

18.1 g (0.1 mol) of 2-ethoxycarbonylaminomethyl-pyrimidine are added to a suspension of 20 g (0.3 mol) of pulverized KOH and 1.1 g (5 mmol) of triethylbenzylammoniumbromide in 200 g of toluene, and then 18 g (0.12 mol) of propargylbromide (80% solution in toluene) at room temperature. The mixture is subsequently stirred for 15 hours at room temperature, the salts are filtered off with suction, the filtrate is washed with brine, dried with MgSO4 concentrated and distilled. The reaction product is identical with that of example Z1b.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312823
Source datasetuspto-grants-1994_05
ORD IDord-f460d2f9ba3c49f892270fb0fc4022df
Source noteuspto-grants-1994_05