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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203124Generated: October 30, 2026

L-Valine → (2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acid

https://huagongshe.com/reaction/2203124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-ValineHCID 6287—
ReactantMethyl chloroformateHCID 6586—
ReactantSodium CarbonateHCID 10340—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
Product(2S)-2-((methoxycarbonyl)amino)-3-methylbutanoic acidHCID 1094296693%

Reaction Steps

Methylchloroformate (14.5 mL, 0.188 mol) was added over 15 min to a cooled (0-6° C.) mixture of (S)-2-amino-3-methyl-butyric acid (20.0 g, 0.171 mol), NaOH (6.80 g, 0.171 mol) and sodium carbonate (18.1 g, 0.171 mol) in water (200 mL). The cooling bath was removed and the mixture was stirred at ambient temperature overnight. Conc. aqueous HCl (30 mL) was added to the reaction mixture to adjust pH to ˜1. A solid formed and the mixture was stirred for 90 min. The mixture was filtered and the solid was dried overnight under reduced pressure at 40° C. t to provide the title intermediate (27.8 g, 93% yield). 1H NMR (CD3OD, 400 MHz) δ (ppm) 4.87 (br. s, 2H), 4.05 (d, J=5.49, 1H), 3.65 (s, 3H), 2.25-2.05 (m, 1H), 0.98 (d, J=6.87, 3H), 0.94 (d, J=6.87, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365549B2
Source datasetuspto-grants-2016_06
ORD IDord-7875122d5ee847e5a8dbd36dd276a304
Source noteuspto-grants-2016_06