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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020880Generated: November 1, 2026

Methyl 4-nitrobutyrate → HCID 57518510, compound

https://huagongshe.com/reaction/1020880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-nitrobutyrateHCID 25604—
Reactant2,5-DifluorobenzaldehydeHCID 137663—
ReactantAmmonium AcetateHCID 517165—
SolventEthanolHCID 702—
ProductHCID 57518510HCID 57518510—

Reaction Steps

To a solution of 2,5-difluorobenzaldehyde (3.82 mL, 35.2 mmol) in ethanol (70 mL) was added methyl 4-nitrobutyrate (4.51 mL, 35.2 mmol) and the mixture was stirred for 5 minutes. To the reaction mixture was added ammonium acetate (5.42 g, 70.4 mmol) and the mixture stirred for 10 minutes at ambient temperature and then heated at reflux temperature for 16 h. The solvent was removed in vacuo and to the yellow oil was added saturated aqueous sodium hydrogen carbonate (100 mL) and the aqueous phase extracted with ethyl acetate (3×50 mL). The combined organic phases were washed with saturated aqueous brine (1×50 mL), dried with anhydrous sodium sulfate, filtered and the solvent removed in vacuo. The yellow racemic product was purified by preparative HPLC on a Berger SFC using ChiralPak AS-H™ column, eluting with 20% MeOH/CO2 to give (5R,6S)-6-(2,5-difluorophenyl)-5-nitropiperidin-2-one [LC/MS 257.1 (M+1)] as the second eluting isomer and the title compound as the first eluting isomer. LC/MS 257.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716482B2
Source datasetuspto-grants-2014_05
ORD IDord-af0d94972a7a435e9f137c1ffa3c2ade
Source noteuspto-grants-2014_05