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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65862Generated: October 26, 2026

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

https://huagongshe.com/reaction/65862

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzyl azidoformateHCID 117521—
ReactantMagnesium monoxideHCID 6850729—
Reactant2-Methylene-5-aminopentanoic acid hydrochlorideHCID 12774425—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product2-Methylene-5-(p-methoxybenzyloxycarbonyl)aminopentanoic acidHCID 13548122116.8%

Reaction Steps

To a solution of 8.8 g of 2-methylene-5-aminopentanoic acid hydrochloride 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 2 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 2 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 numberUS04129571
Source datasetuspto-grants-1978_12
ORD IDord-066bcb46f0dd4fef99e395882e23bb33
Source noteuspto-grants-1978_12