HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199355Generated: October 29, 2026
Formaldehyde → Methyl 1-methylpyrrolidine-2-carboxylate
https://huagongshe.com/reaction/2199355
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Methyl DL-prolinate | HCID 94239 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 1-methylpyrrolidine-2-carboxylate | HCID 529062 | — |
Reaction Steps
Methyl pyrrolidine-2-carboxylate 10b crude product (5 g) was dissolved in 100 mL of methanol. The solution was cooled to 0-5° C. in an ice-water bath, followed by addition of 13 mL of 40% formaldehyde. The reaction mixture was warmed up to room temperature and stirred for 2 hours, then cooled to 0-5° C. in an ice-water bath, and sodium cyanoborohydride (5.45 g, 87.20 mmol) was added in batches. The reaction mixture was warmed up to room temperature and stirred for 24 hours. The mixture was concentrated under reduced pressure and added with 5 mL of water, extracted with dichloromethane (5 mL×3). The combined organic extracts were dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to obtain methyl 1-methylpyrrolidine-2-carboxylate 10c (4.7 g, yield 70.1) crude product as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09358227B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-a749d6dee02341f1ab6cf487c828680f |
|---|
| Source note | uspto-grants-2016_06 |
|---|