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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591182Generated: October 31, 2026

4-Nitrobenzyl bromide → HCID 19045334, compound

https://huagongshe.com/reaction/1591182

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzyl bromideHCID 66011—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 19045273HCID 19045273—
ReactantChloroform methanolHCID 21584188—
SolventDimethylformamideHCID 6228—
ProductHCID 19045334HCID 1904533459.6%

Reaction Steps

A solution of 4-nitrobenzyl bromide (0.73 g, 3.4 mmol), 3,4-dihydro-6-acetamido spiro[(2H)-benzopyran-2,4'-piperidine]-4-one (0.94 g, 3.4 mmol) and diisopropylethylamine (0.61 ml, 3.5 mmol) in dimethylformamide (15 ml) was stirred at room temperature for 3 hr. The reaction mixture was then concentrated under reduced pressure. The residue was diluted with methylene chloride and washed with saturated sodium bicarbonate solution, water and brine. Drying and solvent evaporation gave an oil; flash chromatography (silica gel, methanol-chloroform 2/98) gave 3,4-dihydro-6-acetamido-1'-(4-nitrobenzyl)spiro[(2H)-1-benzopyran-2,4'-piperidine]-4-one (0.83 g, 59%); 75 mg converted to hydrochloride; mp>250° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05206240
Source datasetuspto-grants-1993_04
ORD IDord-14bc5a263d1a4892bc0fcf6a64e28a43
Source noteuspto-grants-1993_04