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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265268Generated: November 1, 2026

L-Leucine → L-Leucine, N-((1,1-dimethylethoxy)carbonyl)-

https://huagongshe.com/reaction/1265268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-LeucineHCID 6106—
ReactantSodium HydroxideHCID 14798—
ReactantDi-tert-butyl dicarbonateHCID 90495—
SolventDiethyl EtherHCID 3283—
ProductL-Leucine, N-((1,1-dimethylethoxy)carbonyl)-HCID 83170—

Reaction Conditions

Temperature23 °C

Reaction Steps

To the suspension of 10 g (76.2 mmol ) of L-leucine in 140 mL of diethyl ether was added 80 mL of 10% NaOH. After all solid dissolves, 20 mL (87.1 mmol) of BOC2O was added to the reaction mixture. The resulting reaction mixture was stirred at 23° C. for 12 h. After this period, the layers were separated and the aqueous layer was acidified to pH 1 by careful addition of 1N aqueous HCl at 0° C. The resulting mixture was extracted with ethyl acetate (3×100 mL). The organic layers were combined and washed with brine and dried over anhydrous Na2SO4. The solvent was removed under reduced pressure to provide title product which was used directly for next reaction without further purification (yield, 97%). 1H NMR (400MHz, CDCl3) δ 4.89 (broad d, 1H, J =8.3 Hz), 4.31 (m, 1H), 1.74-1.49 (m, 3H), 1.44 (s, 9H), 0.95 (d, 6H, J=6.5 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06545127B1
Source datasetuspto-grants-2003_04
ORD IDord-0b464dc79e824a7687c7b45f136efcd3
Source noteuspto-grants-2003_04