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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352761Generated: November 3, 2026

N-methyl-2-pyrrolidone → 4-(2-Hydroxymethyl-1-pyrrolidinyl)-2-nitrobenzoic acid methyl ester

https://huagongshe.com/reaction/1352761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantMethyl 4-chloro-2-nitrobenzoateHCID 39135—
ReactantDiisopropylethylamineHCID 81531—
ReactantL-ProlinolHCID 640091—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product4-(2-Hydroxymethyl-1-pyrrolidinyl)-2-nitrobenzoic acid methyl esterHCID 69264246998.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-chloro-2-nitrobenzoic acid methyl ester 100 mg, prolinol 56 mg, diisopropylethylamine 90 mg and 1-methyl-2-pyrrolidinone 3 ml is stirred at 100° C. for 13 hours. Ethyl acetate and water are added to the mixture, and the organic layer is washed with water (twice) and brine, and dried over sodium sulfate. After removal of the sodium sulfate, the filtrate is concentrated in vacuo, and the residue is purified with column chromatography (silica gel 100 g, solvent; hexane:ethyl acetate=4:1→2:1→1:1→100% ethyl acetate) to give 4-(2-hydroxymethyl-1-pyrrolidinyl)-2-nitrobenzoic acid methyl ester 1.298 g as a pale yellow viscosity oil. MS(m/z): 285(M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220736B2
Source datasetuspto-grants-2007_05
ORD IDord-efd6ec66bcf741b082ddb75b890f97f6
Source noteuspto-grants-2007_05