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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | L-Proline | HCID 145742 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (S)-Methyl 1-methylpyrrolidine-2-carboxylate | HCID 10920622 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05424444 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-f35bf35630634bafb7fa2eff30a2d559 |
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| Source note | uspto-grants-1995_06 |
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