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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372573Generated: October 30, 2026

Triethylamine → BOC-p-nitrophenylalanine 2-oxopropyl amide

https://huagongshe.com/reaction/2372573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant2-Propanone, 1-amino-, hydrochlorideHCID 3084025—
ReactantN-(tert-Butoxycarbonyl)-4-nitro-L-phenylalanineHCID 7021882—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
ProductBOC-p-nitrophenylalanine 2-oxopropyl amideHCID 18632424—

Reaction Conditions

Temperature0 °C

Reaction Steps

t-Butyloxycarbonyl-p-nitrophenylalanine (4.42g, 14.26 mmol, aminoacetone hydrochloride (1.56 g, 14.26 mmol), triethylamine (1.44 g, 14.26 mmol), 1-hydroxybenzotriazole (1.69 g, 12.55 mmol), were dissolved in ethyl acetate (400 ml). 1,3-Dicyclohexylcarbodiimide (3.23 g, 15.68 mmol) in ethyl acetate (25 ml) was added and the solution allowed to stir for 18 hours. Glacial acetic acid (0.2 ml) was added and the solution was filtered. The filtrate was extracted with saturated salt solution (100 ml), lN HCl solution (3×100 ml), and saturated salt solution (100 ml), 5% bicarbonate solution (3×100 ml), and saturated salt solution (100 ml). The organic phase was dried over MgSO4 , filtered and concentrated to 50 ml. Petroleum ether (50 ml) was added and the solution was cooled to 0° C. for 12 hours. The precipitated product was collected and dried under vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05099069
Source datasetuspto-grants-1992_03
ORD IDord-c98996705224496485137af2027e84e9
Source noteuspto-grants-1992_03