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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36127Generated: October 25, 2026

Ethanol → N-Boc-4-cyanophenylalanine-N-methylamide

https://huagongshe.com/reaction/36127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMethylamineHCID 6329—
Reactant4-MethylmorpholineHCID 7972—
ReactantPentafluorophenolHCID 13041—
ReactantN-(tert-Butoxycarbonyl)-4-cyano-L-phenylalanineHCID 7020841—
SolventDichloromethaneHCID 6344—
ProductN-Boc-4-cyanophenylalanine-N-methylamideHCID 2285121092%

Reaction Steps

A solution of N-Boc-4-cyanophenylalanine (1.92 g, 6.6 mmol) and pentafluorophenol (2.43 g, 13.2 mmol) in CH2Cl2 (30 ml) at 0° C. was treated with 4-methylmorpholine (0.74 g, 7.3 mmol). After stirring the reaction mixture for 3 hours, 8M methylamine in ethanol (15 ml, 19.8 mmol) was added and the reaction mixture left to stir at room temperature for 16 hours. The solvent was removed under pressure, the residue dissolved in CH2Cl2 (50 ml) and washed with saturated sodium bicarbonate (2×50 ml), 1M citric acid (2×50 ml) and brine (50 ml). The CH2Cl2 layer was dried over MgSO4 and the solvent removed under pressure to yield the title compound as a white solid (1.84 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05412145
Source datasetuspto-grants-1995_05
ORD IDord-a67bf3e8d4a2491c9a876d6e5cb62b11
Source noteuspto-grants-1995_05