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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463548Generated: October 25, 2026

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

https://huagongshe.com/reaction/1463548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
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 methylazine 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 numberUS05300674
Source datasetuspto-grants-1994_04
ORD IDord-9949f6ba5f064ab3845911c82f62e8b6
Source noteuspto-grants-1994_04