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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071994Generated: October 31, 2026

Acetic Anhydride → N-[[1-(4-Methyl-1-piperazinyl)cyclohexyl]methyl]formamide

https://huagongshe.com/reaction/2071994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant1-[1-(4-METHYLPIPERAZIN-1-YL)CYCLOHEXYL]METHANAMINEHCID 7018132—
SolventFormic AcidHCID 284—
ProductN-[[1-(4-Methyl-1-piperazinyl)cyclohexyl]methyl]formamideHCID 2140985866.3%

Reaction Steps

Formic acid (6.9 g, 0.15 mole) and acetic anhydride (15.3 g, 0.15 mole) were mixed without cooling and kept at room temperature for 1 hr. 1-(1-aminomethylcyclohexyl)-4-methylpiperazine (8.4 g, 0.04 mole) was dissolved in formic acid (12 ml) and the formylating mixture (16 ml) added. This produced vigorous effervescence and a rise in temperature to 70°. The mixture was left at room temperature for 2 hr. and then heated on a water bath at 55° for 0.75 hr. The solvents were removed under reduced pressure yielding a viscous brown oil (6.0 g, 66.3%) which crystallised as colourless plates of 1-(1-formylaminomethylcyclohexyl)-4-methylpiperazine from light petroleum (b.p. 80°-100°), m.p. 97°-98°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04049663
Source datasetuspto-grants-1977_09
ORD IDord-69564f4983524fc0bb2c75310232072a
Source noteuspto-grants-1977_09