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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371014Generated: October 29, 2026

Dimethyl Sulfoxide → N-(tert-Butoxycarbonyl)-4-carbamoyl-2,6-dimethyl-L-phenylalanine

https://huagongshe.com/reaction/2371014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantHydrogen PeroxideHCID 784—
ReactantPotassium CarbonateHCID 11430—
Reactant(S)-methyl 2-((tert-butoxycarbonyl)amino)-3-(4-cyano-2,6-dimethylphenyl)propanoateHCID 46218695—
SolventWaterHCID 962—
ProductN-(tert-Butoxycarbonyl)-4-carbamoyl-2,6-dimethyl-L-phenylalanineHCID 11847987—

Reaction Steps

A 50 mL three-necked round bottom flask equipped with magnetic stirrer, and thermocouple was charged under nitrogen with (S)-2-tert-butoxycarbonylamino-3-(4-cyano-2,6-dimethyl-phenyl)-propionic acid methyl ester (166.2 mg, 0.5 mmol), DMSO (5.0 mL), and K2CO3 (75 mg, 0.5 mmol) and the resulting mixture cooled in an ice bath. To the resulting mixture was then added 30% H2O2 (110 μl), dropwise via a syringe. The resulting mixture was then allowed to warm up to ambient temperature, with the solids observed to dissolve to yield a clear solution. After stirring for about 2 hours at 45-50° C., water (10 mL) was added, cooling was applied, and a precipitated product isolated by filtration. The isolated white solid was washed with water (2×25 mL), then dried for 24 hours on high vacuum pump to yield the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710256B2
Source datasetuspto-grants-2014_04
ORD IDord-ac98cc9a3c204299bfeb198a140e7d6f
Source noteuspto-grants-2014_04