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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21755Generated: October 25, 2026

Formaldehyde → (S)-Methyl 1-methylpyrrolidine-2-carboxylate

https://huagongshe.com/reaction/21755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantPotassium CarbonateHCID 11430—
ReactantL-ProlineHCID 145742—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product(S)-Methyl 1-methylpyrrolidine-2-carboxylateHCID 10920622—

Reaction Conditions

Temperature0 °C

Reaction Steps

The L-proline is dissolved in methanol, the solution is cooled to 0° C. and 36% aqueous formaldehyde is added with stirring. To this solution is then added powdered NaBH4 in portions while maintaining the temperature between -5° and +5° C. The reaction is filtered, the filter cake extracted with solvent and combined with the filtrate, and the solvents evaporated to dryness. The residual N-methyl-L-proline is then dissolved in and reacted with methanol in the presence of H2SO4 at reflux for 4-24 hr. The reaction mixture is cooled to 0° C., and with vigorous stirring a solution of K2CO3 is slowly added to the mixture, until the pH is between pH 7 and 8, then the title product is extracted from the basic mixture and isolated after drying and removal of the solvent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05424444
Source datasetuspto-grants-1995_06
ORD IDord-f35bf35630634bafb7fa2eff30a2d559
Source noteuspto-grants-1995_06