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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638673Generated: October 30, 2026

Methanol → 3-Methoxymethyl-2,5-difluoro-4-(4-ethoxycarbonyl-1-piperazinyl)nitrobenzene

https://huagongshe.com/reaction/1638673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant3,6-Difluoro-2-(4-ethoxycarbonyl-1-piperazinyl)-5-nitrobenzyl alcoholHCID 15622528—
Product3-Methoxymethyl-2,5-difluoro-4-(4-ethoxycarbonyl-1-piperazinyl)nitrobenzeneHCID 19841148—

Reaction Steps

3,6-Difluoro-2-(4-ethoxycarbonyl-1-piperazinyl)-5-nitrobenzyl alcohol (7.14 g) is dissolved in methanol (770 ml), and thereto is added dropwise conc. sulfuric acid (145 ml) while cooling on an ice bath. The mixture is refluxed for 4 hours. The reaction mixture is cooled to room temperature and is poured into ice water (1.5 liter), and then extracted with dichloromethane. The extract is dried over magnesium sulfate and sodium sulfate, and then the solvent is distilled off under reduced pressure to give 3-methoxymethyl-2,5-difluoro-4-(4-ethoxycarbonyl-1-piperazinyl)nitrobenzene (7.39 g) as yellow powder, m.p. 85°-86° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04880806
Source datasetuspto-grants-1989_11
ORD IDord-7eb682215e504b34881307011c291da5
Source noteuspto-grants-1989_11