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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167579Generated: October 28, 2026

Formic Acid → HCID 22712051, compound

https://huagongshe.com/reaction/1167579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantFormaldehydeHCID 712—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 22712046HCID 22712046—
SolventMethanolHCID 887—
ProductHCID 22712051HCID 22712051—

Reaction Conditions

Temperature95 °C

Reaction Steps

From 47.4 g of 1-benzyl-4-(3-hydroxypropylamino)-piperidine-dihydrochloride the base is liberated, combined with 63 ml of 85% formic acid and 22 ml of 37% formaldehyde solution and stirred for two hours at about 90-100° C. The mixture is left to cool, 37 ml of formic acid and 11 ml of formaldehyde solution are added and it is stirred for another hour at about 100-110° C. It is left to cool, combined with 150 ml of methanol, made alkaline with about 270 ml of 32% sodium hydroxide solution with cooling and stirred for about another 30 minutes at 40-50° C. and then the methanol is distilled off. The residue is extracted with twice 100 ml of methylene chloride, the combined methylene chloride phases are dried, filtered and freed from solvent in vacuo. The residue is taken up in 80 ml Ethanol, acidified with 34 ml of 32% hydrochloric acid, combined with 100 ml of acetone and stirred. As soon as crystals have been precipitated more acetone is added. The precipitate is suction filtered, washed with acetone and dried. 42.8 g of 1-benzyl-4-[-(3-hydroxypropyl)-methylamino]-piperidine-dihydrochloride are obtained in the form of a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620438B2
Source datasetuspto-grants-2003_09
ORD IDord-68b0fce035714109bc21aa9ca6a7ee69
Source noteuspto-grants-2003_09