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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351379Generated: October 31, 2026

Formaldehyde → HCID 14209985, compound

https://huagongshe.com/reaction/2351379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantCyclohexaneHCID 8078—
ReactantSodium CyanideHCID 8929—
ReactantN,N-Diethyl-2-piperidinemethanamineHCID 254287—
ReactantSodium BisulfiteHCID 23665763—
SolventWaterHCID 962—
ProductHCID 14209985HCID 1420998599%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 236.5 ml (about 1.1 mol) of a 37% aqueous sodium hydrogen sulphite solution and 110 ml (about 1.1 mol) of a 40% formalin solution was heated to 60° C. for 30 minutes. It was allowed to cool to 30° C., a solution of 170.3 g (1.0 mol) of 2-[(diethylamino)methyl]piperidine in 70 ml of water was added dropwise thereto, whereupon the mixture spontaneously heated up to 40° C., and was then stirred for a further 2 hours without any external heating. The solution of 53.9 g (1.1 mol) of sodium cyanide in 172 ml of water was then added and the resulting mixture was stirred for 2 hours at ambient temperature. The upper organic layer was taken up in 500 ml of cyclohexane and the aqueous phase was extracted four times, each time with 125 ml of cyclohexane. The combined extracts were dried over sodium sulphate, concentrated by evaporation and distilled in vacuo. The desired 2-[2-[(diethylamino)methyl]-piperidin-1-yl]acetonitrile was obtained as a colourless oil, B.p.19 mm Hg 155°-156° C. in a yield of 172.0 g (82% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873236
Source datasetuspto-grants-1989_10
ORD IDord-a0d2a8e0b7ab4d09b87d3f4eeb2f2857
Source noteuspto-grants-1989_10