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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397071Generated: November 3, 2026

Formaldehyde → Methyl 1-methylpyrrolidine-2-carboxylate

https://huagongshe.com/reaction/1397071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantMethyl DL-prolinateHCID 94239—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
ProductMethyl 1-methylpyrrolidine-2-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901140B2
Source datasetuspto-grants-2014_12
ORD IDord-ad7b6aed354a4a628bdc7e245218c1ba
Source noteuspto-grants-2014_12