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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007283Generated: October 28, 2026

Dimethylformamide → Methyl-2-[(t-butoxycarbonyl)amino]-3-[-(4-formylphenoxy) phenyl]propanoate

https://huagongshe.com/reaction/1007283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantMethyl 2-((tert-butoxycarbonyl)amino)-3-(4-hydroxyphenyl)propanoateHCID 4459028—
ProductMethyl-2-[(t-butoxycarbonyl)amino]-3-[-(4-formylphenoxy) phenyl]propanoateHCID 2266905785%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of fresh sodium hydride (0.813 g, 33.9 mmol) in dry DMF (20 ml) under nitrogen atmosphere was added the solution of methyl-2-[(t-butoxycarbonyl)amino]-3-(4-hydroxyphenyl)propanoate (10 g, 33.9 mmol) in DMF (20 ml) slowly. The mixture was stirred for 15 minutes. 4-Fluorobenzaldehyde (4.20 g, 33.9 mmol) was added and the mixture was heated to 80° C. After completion of the reaction, the solvent was removed by high vacuum and the mixture was quenched with addition of saturated aqueous ammonium chloride. The mixture was extracted with ethyl acetate (3×50 ml). After washing with brine and dried on anhydrous sodium sulfate, the solvent was evaporated and the product was purified with flash column from eluent of hexanes: ethyl ether; 12/30 to 12/22 to afford the title compound as an oil (yield 11.5 g, 85.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794401B2
Source datasetuspto-grants-2004_09
ORD IDord-20903513c1ef421cb45a4945af91f8d9
Source noteuspto-grants-2004_09