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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781384Generated: October 31, 2026

4-Nitrobenzyl bromide → HCID 19045334, compound

https://huagongshe.com/reaction/1781384

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-acetamidospiro[(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 numberUS05633247
Source datasetuspto-grants-1997_05
ORD IDord-947d6841260549d3b54d67fb4a7179a9
Source noteuspto-grants-1997_05