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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852650Generated: October 30, 2026

Methanol → 3-Nitro-5-(2-oxo-piperidin-1-yl)-benzoic acid methyl ester

https://huagongshe.com/reaction/852650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium hydrideHCID 24758—
Reactant3-(5-Chloro-pentanoylamino)-5-nitro-benzoic acid methyl esterHCID 69357073—
SolventTetrahydrofuranHCID 8028—
Product3-Nitro-5-(2-oxo-piperidin-1-yl)-benzoic acid methyl esterHCID 6935761853%

Reaction Steps

NaH (60% w/w in mineral oil, 680 mg, 17 mmol, 0.9 equiv) was added portionwise to a solution of 3-(5-chloro-pentanoylamino)-5-nitro-benzoic acid methyl ester (D3) (6 g, 19 mmol, 1 equiv) in THF (40 ml) under nitrogen. The resulting mixture was stirred at room temperature for 1 h and then MeOH was added dropwise. The solution was concentrated in vacuo and the residue diluted with AcOEt. The organic phase was washed with H2O, dried over MgSO4 and concentrated in vacuo. Purification by flash chromatography on silica gel (AcOEt/iso-hexane: 1/2) gave 3-nitro-5-(2-oxo-piperidin-1-yl)-benzoic acid methyl ester (B82) (2.8 g, 53%) as a pale orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253198B2
Source datasetuspto-grants-2007_08
ORD IDord-a70fad6f219f4ff78432b0abcb0922ae
Source noteuspto-grants-2007_08