HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261327Generated: October 26, 2026
4-Methoxybenzyl azidoformate → 2-Methylene-5-(p-methoxybenzyloxycarbonyl)aminopentanoic acid
https://huagongshe.com/reaction/261327
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methoxybenzyl azidoformate | HCID 117521 | — |
| Reactant | Magnesium monoxide | HCID 6850729 | — |
| Reactant | 2-Methylene-5-aminopentanoic acid hydrochloride | HCID 12774425 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Methylene-5-(p-methoxybenzyloxycarbonyl)aminopentanoic acid | HCID 13548122 | 116.8% |
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 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04165320 |
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| Source dataset | uspto-grants-1979_08 |
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| ORD ID | ord-34cbf9ce17eb47b7b515846a13eaa014 |
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| Source note | uspto-grants-1979_08 |
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