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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 126837Generated: October 26, 2026

Carbon Dioxide → 2-(4-Fluoro-1-piperidylmethyl)propenenitrile

https://huagongshe.com/reaction/126837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantFormaldehydeHCID 712—
ReactantCyanoacetic acidHCID 9740—
ReactantSodium BicarbonateHCID 516892—
Reactant4-FluoropiperidineHCID 2759159—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product2-(4-Fluoro-1-piperidylmethyl)propenenitrileHCID 13041034—

Reaction Conditions

Temperature65 °C

Reaction Steps

4-Fluoropiperidine (0.7 g., 0.005 mole) was dissolved in a mixture of 3 ml. of dioxane and 2 ml. of water containing cyanoacetic acid (0.43 g., 0.005 mole). Then, 0.85 g. (0.01 mole) of 37% aqueous formaldehyde was added to the solution. The solution was heated to 65° C. and carbon dioxide evolution began. It was maintained at 60°-65° C. for 21/2 hours and allowed to stand overnight. A solid gummy residue, 1 gm., was obtained upon stripping in a bath at 55° C. and at 1 mm. It was taken up in a small amount of water, made alkaline with sodium bicarbonate and extracted with ether. The organic layer was water washed and dried over anhydrous sodium sulfate. After solvent stripping, the product was obtained as a colorless oil, 0.7 g., of analytical purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04254131
Source datasetuspto-grants-1981_03
ORD IDord-bbf5626a65f8497384b49ee61d97e8ac
Source noteuspto-grants-1981_03