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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750929Generated: November 2, 2026

Sodium Carbonate → 3,3-dimethyl-2-(phenylmethoxycarbonylamino)butanoic acid

https://huagongshe.com/reaction/1750929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantBenzyl chloroformateHCID 10387—
ReactantL-tert-LeucineHCID 164608—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
Product3,3-dimethyl-2-(phenylmethoxycarbonylamino)butanoic acidHCID 3401206817.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of L-tert-leucine (1) (50.0 g, 38.0 mmol) and NaHCO3 (96.0 g, 114 mmol) in ice (500 g) and water (500 ml) was added benzyl chloroformate (65.0 ml, 74.0 mmol) and the reaction stirred at 0° C. for 3 hours then at room temperature for 18 hours. 0.1N Na2CO3 was added until the oily layer dissolved and the solution was washed with 10% EtOAc in hexanes (2×500 ml). The iced aqueous phase was acidified to pH 1 using 12N HCl then extracted using EtOAc (3×350 ml). The combined organic extracts were dried over Na2SO4, filtered and evaporated to give the title compound as a colorless oil (82.4 g, 81.5% yield): 1H-NMR (500 MHz, CDCl3) δ1.02 (s, 9H), 4.22 (d, 1H), 5.10-5.14 (m, 2H), 5.31 (d, 1H), 7.26-7.37 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156880B2
Source datasetuspto-grants-2015_10
ORD IDord-ce07fe27072e4ef1a26bf1861c554761
Source noteuspto-grants-2015_10