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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844866Generated: November 1, 2026

Formaldehyde → (R)-tert-Butyl 1-methylpyrrolidin-3-ylcarbamate

https://huagongshe.com/reaction/1844866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantMethanolHCID 887—
Reactant(3R)-(+)-3-(tert-Butoxycarbonylamino)pyrrolidineHCID 1514397—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
Product(R)-tert-Butyl 1-methylpyrrolidin-3-ylcarbamateHCID 4509194259.4%

Reaction Steps

In a dried reaction flask, (R)-tert-butyl pyrrolidin-3-ylcarbamate (5.774 g, 31.0 mmol) and formaldehyde solution (37%, 6.82 mL) were dissolved into methanol (124 mL) under a nitrogen protection. The mixture was stirred at room temperature for 1 hr. Sodium borohydride (3.518 g, 93.0 mmol) was added in portion under an ice bath. The mixture was stirred at room temperature for 3 hr. Water was added and the solution was concentrated under reduced pressure. Ethyl acetate and saturated aqueous sodium bicarbonate solution were added. The mixture was extracted with ethyl acetate. The combined organic phase was washed with brine, dried over anhydrous sodium sulfate, filtered, purified by silica gel column chromatography (ethyl acetate:petroleum ether=1:1) to produce a white solid (3.685 g) in 59.4% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946279B2
Source datasetuspto-grants-2015_02
ORD IDord-9339ebcb5d9c43e58680193ea60ff4a9
Source noteuspto-grants-2015_02