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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426996Generated: November 2, 2026

Acetic Acid → 2-tert-Butoxycarbonylamino-3-(4-fluoro-phenylamino)-2-methyl-propionic acid methyl ester

https://huagongshe.com/reaction/2426996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-FluoroanilineHCID 9731—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantMethyl 2-[(tert-butoxycarbonyl)amino]-2-methyl-3-oxopropanoateHCID 22630101—
SolventMethanolHCID 887—
Product2-tert-Butoxycarbonylamino-3-(4-fluoro-phenylamino)-2-methyl-propionic acid methyl esterHCID 5767892353.2%

Reaction Steps

To a solution of 2-tert-butoxycarbonylamino-2-methyl-3-oxo-propionic acid methyl ester (2.35 g, 6.71 mmol) in methanol (25 mL) was added 4-fluoroaniline (0.53 mL, 5.59 mmol) and acetic acid (0.16 mL, 2.80 mmol). A solution of sodium cyanoborohydride (188 mg, 2.99 mmol) in methanol (25 mL) was added dropwise and the reaction mixture stirred for 3 hours at room temperature post addition. The solvent was removed in vacuo and the residue dissolved in DCM (50 mL). The organic solution was treated with aqueous sodium carbonate solution (20 mL, 1N), stirred for 20 min, and the aqueous layer removed. Concentration of the organic layer followed by purification of the residue using flash chromatography (SiO2, DCM) afforded the title compound as a yellow oil (970 mg, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968580B2
Source datasetuspto-grants-2011_06
ORD IDord-cb22fab201d740328527ac7f1ba3edac
Source noteuspto-grants-2011_06