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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3672Generated: October 23, 2026

Benzyl chloroformate → 2-{[(Benzyloxy)carbonyl]amino}-3-(thiophen-2-yl)propanoic acid

https://huagongshe.com/en/reaction/3672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantPotassium CarbonateHCID 11430—
Reactant2-ThienylalanineHCID 91444—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product2-{[(Benzyloxy)carbonyl]amino}-3-(thiophen-2-yl)propanoic acidHCID 1280683098%

Reaction Steps

To a mixture of 3.0 g (16.9 mmol) of β-thienyl-D,L-alanine in 75 mL of water and 60 mL of dioxane, was added 5.6 g (40.6 mmol) of anhydrous potassium carbonate, followed by 2.85 mL (20 mmol) of carbobenzyloxychloride. The resulting mixture was stirred rapidly for approximately one hour. When the reaction was substantially complete, as indicated by thin layer chromatography (21/7/7/9, EtOAc/AcOH/CH3 CN/H2O), the reaction mixture was concentrated. The resultant layers were separated and the aqueous layer was washed with 75 mL of diethyl ether and then layered with 150 mL of methylene chloride. The resultant mixture was acidified with rapid stirring to pH=2.0 using 5N hydrochloric acid. The layers were then separated, and the organic layer was dried with sodium sulfate (Na2SO4), filtered and concentrated to provide 5.05 g of desired compound (98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05734057
Source datasetuspto-grants-1998_03
ORD IDord-608e80bb9092458b8ead7e8d78854485
Source noteuspto-grants-1998_03