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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894885Generated: October 30, 2026

4-Methoxybenzyl azidoformate → 2-Methylene-5-(p-methoxybenzyloxycarbonyl)aminopentanoic acid

https://huagongshe.com/reaction/894885

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzyl azidoformateHCID 117521—
ReactantMagnesium monoxideHCID 6850729—
Reactant2-Methylene-5-aminopentanoic acidHCID 12774424—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product2-Methylene-5-(p-methoxybenzyloxycarbonyl)aminopentanoic acidHCID 13548122105.4%

Reaction Steps

To a solution of 8.8 g of 2-methylene-5-aminopentanoic acid hydrochloric in 100 ml of water is added with stirring 6.36 g of magnesium oxide, followed by a solution of 12.2 g of p-methoxybenzyloxycarbonyl azide in 100 ml of dioxane, and the resulting mixture is stirred at room temperature for two days. The reaction mixture is filtered, and the filtrate diluted with 200 ml of ethyl acetate, two equivalents of Dowex 50 ion exchange resin is added, and the mixture is stirred at room temperature for two hours. The resin is then filtered off and washed with water. The layers in the filtrate are separated and the aqueous layer is extracted twice with ethyl acetate. The combined organic layers are dried and concentrated in vacuo to give 18.2 g of 2-methylene-5-(p-methoxybenzyloxycarbonyl)aminopentanoic acid as an amber oil which crystallizes on standing. This is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04284779
Source datasetuspto-grants-1981_08
ORD IDord-fea3093f741d404a8a43bcd24d6d45d6
Source noteuspto-grants-1981_08