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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888772Generated: November 2, 2026

Triethylamine → Tert-butyl (2-{[4-(benzyloxy)-2-nitrophenyl]amino}-1-methyl-2-oxoethyl)carbamate

https://huagongshe.com/reaction/1888772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
Reactant4-Benzyloxy-2-nitroanilineHCID 261497—
Reactant2-N-Boc-aminopropionic acidHCID 268471—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl (2-{[4-(benzyloxy)-2-nitrophenyl]amino}-1-methyl-2-oxoethyl)carbamateHCID 12378917999.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of N-(tert-butoxycarbonyl)-D,L-alanine (3.49 g, 18.4 mmol) and triethylamine (2.56 mL, 18.4 mmol) in THF (100 mL) was added 2-methylpropyl chlorocarbonate (2.39 mL, 18.4 mmol) under ice-cooling, and the mixture was stirred for 30 min. To this solution was added 4-(benzyloxy)-2-nitroaniline (3.00 g, 12.3 mmol), and the mixture was heated under reflux at 90° C. for 16 hr under a nitrogen atmosphere. After being allowed to cool to room temperature, the reaction mixture was diluted with ethyl acetate, and the mixture was washed with 0.5N hydrochloric acid, 10% aqueous potassium carbonate solution and saturated brine, and dried over anhydrous sodium sulfate. This solution was applied to basic silica gel column chromatography (ethyl acetate). The solvent was evaporated under reduced pressure to give tert-butyl (2-{[4-(benzyloxy)-2-nitrophenyl]amino}-1-methyl-2-oxoethyl)carbamate (5.10 g) as a crude product. To a solution (66 mL) of the obtained oil (5.10 g, 12.3 mmol) in 90% aqueous acetic acid was slowly added zinc powder (8.03 g, 123 mmol) under ice-cooling, and the mixture was stirred for 30 min. The reaction mixture was filtered through celite, and the filtrate was stirred under heating at 70° C. for 2 hr. The reaction mixture was allowed to cool to room temperature, and the solvent was evaporated under reduced pressure. The obtained residue was diluted with ethyl acetate, and the mixture was washed with 10% aqueous potassium carbonate solution and saturated brine, and dried over anhydrous sodium sulfate. The solution was applied to basic silica gel column chromatography (ethyl acetate), and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1 to ethyl acetate), and triturated with diisopropyl ether to give the title compound (663 mg, yield in 3 steps 15%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501804B2
Source datasetuspto-grants-2013_08
ORD IDord-1ef5b72456b14b3489fc8afa94414761
Source noteuspto-grants-2013_08