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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600201Generated: October 30, 2026

Methyl 4-nitrobutyrate → HCID 19075158, compound

https://huagongshe.com/reaction/1600201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-nitrobutyrateHCID 25604—
ReactantAmmonium AcetateHCID 517165—
Reactant3-(Trifluoromethoxy)benzaldehydeHCID 605139—
SolventEthanolHCID 702—
ProductHCID 19075158HCID 1907515899.9%

Reaction Steps

Under a nitrogen atmosphere, in a round-bottom flask were placed 15 g (79 mmol) of 3-trifluoromethoxybenzaldehyde, 80 mL of ethanol, 11 g (0.26 mol)of ammonium acetate and 12.6 mL (79 mmol) of methyl 4-nitrobutyrate, and the mixture was heated at reflux for 6 hours. After cooling to room temperature, the mixture was concentrated. The remaining material was stirred with ca. 200 mL of CHCl3 for 30 minutes, filtered and concentrated. The residue purified by flash column chromatography, elutingwith 1:49 methanol/chloroform followed by 1:19 methanol/chloroform to obtain 24 g of 5-nitro-6-(3-trifluoromethoxyphenyl)piperidin-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05744480
Source datasetuspto-grants-1998_04
ORD IDord-250f255a2add47c4b8d12cf1cac67677
Source noteuspto-grants-1998_04