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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698769Generated: October 25, 2026

Potassium Carbonate → (R)-2-((tert-Butoxycarbonyl)amino)-3-((2-nitrophenyl)amino)propanoic acid

https://huagongshe.com/reaction/1698769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
Reactant3-Amino-N-(tert-butoxycarbonyl)-D-alanineHCID 7020984—
SolventDimethylformamideHCID 6228—
Product(R)-2-((tert-Butoxycarbonyl)amino)-3-((2-nitrophenyl)amino)propanoic acidHCID 5451259899%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 2-fluoronitrobenzene (3.45 g) in N,N-dimethylformamide (60 mL), (R)-(−)-2-tert-butoxycarbonylamino-3-amino-propionic acid (5 g) and potassium carbonate (6.77 g) were added, followed by stirring overnight at 70° C. The reaction mixture was allowed to cool down, poured into ice water, and then extracted with ethyl acetate. After 1 N hydrochloric acid was added to the aqueous layer to adjust pH to 3, the aqueous layer was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous sodium sulfate. The solvent was then evaporated under reduced pressure. n-Hexane was added to the residue to for crystallization. The resultant crystals were collected by filtration, whereby the title compound (7.9 g) was obtained. Yield: 99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06344452B1
Source datasetuspto-grants-2002_02
ORD IDord-19f5d793898a4c83b763ac3eed7429f5
Source noteuspto-grants-2002_02