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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170864Generated: October 31, 2026

Lithium Hydroxide → n-4-Methoxybenzyloxycarbonyl alpha-methyl beta-alanine

https://huagongshe.com/reaction/1170864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
Reactantn-4-Methoxybenzyloxycarbonyl alpha-methyl beta-alanine methyl esterHCID 21879751—
SolventMethanolHCID 887—
Productn-4-Methoxybenzyloxycarbonyl alpha-methyl beta-alanineHCID 1548722197.3%

Reaction Steps

A solution of N-4-methoxybenzyloxycarbonyl α-methyl β-alanine methyl ester (2.81 g, 10.0 mmol) in 30 mL of 25% aqueous methanol was treated with lithium hydroxide (1.3 equivalents) at room temperature for a period of 2 h. The solution was concentrated in vacuo and the residue taken up in a mixture of water and ether and the phases separated and the organic phase discarded. The aqueous phase was acidified with aqueous potassium hydrogen sulfate to pH=1.5 and then extracted three times with ether. The combined ethereal phase was washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to give 2.60 g, 97% of N-4-Methoxybenzyloxycarbonyl α-methyl β-alanine (N-Moz-AMBA) which was purified by recrystallization from a mixture of ethyl acetate and hexane to give 2.44 g, 91% of pure product, mp 96-97° C., MH+=268. 1H NMR (D6-acetone/300 MHz) 1.16 (3H, d, J=7.2 Hz), 2.70 (1H, m), 3.31 (2H, m), 3.31 (3H, s), 4.99 (2H, s), 6.92 (2H, 4, J=8.7 Hz), 7.13 (2H, d, J=8.7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829564B2
Source datasetuspto-grants-2010_11
ORD IDord-a8df30c9bd324db7b209693fcddce32b
Source noteuspto-grants-2010_11