HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → (S)-Methyl 1-methylpyrrolidine-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | methyl L-prolinate hydrochloride | HCID 2733200 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | (S)-Methyl 1-methylpyrrolidine-2-carboxylate | HCID 10920622 | 77% |
Reaction Steps
A 10.42 g (62.92 mmol) sample of L-proline methyl ester hydrochloride (Aldrich Chemical Co.) was reductively methylated over 2.5 g of 10% Pd/C under 4 Atm of hydrogen in a solution containing 20 g of sodium acetate and 49.5 mL of 37% aqueous formaldehyde for 48 hours. Upon completion of the reaction, the methanolic solution was concentrated and the residue was dissolved in 10% aq. HCl (60 mL) and washed with ether (3×100 mL), then the aqueous layer was adjusted to pH ~12 with K2CO3 (solid) and extracted with methylene chloride (3×75 mL). The combined methylene chloride layers were dried (MgSO4) and concentrated to afford the crude product as a clear oil (16.6 g, 77% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05424444 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-f2e5dc8bddec4c22b2776b5f49d6f5af |
| Source note | uspto-grants-1995_06 |