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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335336Generated: October 30, 2026

Triethylamine → (S)-tert-Butyl 2-(2-(methoxymethyl)pyrrolidin-1-yl)ethylcarbamate

https://huagongshe.com/reaction/335336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPotassium CarbonateHCID 11430—
Reactant(S)-(+)-2-(Methoxymethyl)pyrrolidineHCID 671217—
Reactanttert-Butyl N-(2-bromoethyl)carbamateHCID 4103526—
SolventAcetonitrileHCID 6342—
Product(S)-tert-Butyl 2-(2-(methoxymethyl)pyrrolidin-1-yl)ethylcarbamateHCID 71283522—

Reaction Conditions

Temperature85 °C

Reaction Steps

A suspension comprising (S)-2-(methoxymethyl)pyrrolidine (1 g, 8.68 mmol), tert-butyl 2-bromoethylcarbamate (1.946 g, 8.68 mmol), triethylamine (1.210 ml, 8.68 mmol) and potassium carbonate (1.200 g, 8.68 mmol) in MeCN (10 ml) was heated at 85° C. overnight. The resulting mixture was filtered and washed with MeCN. Purification of the crude product by chromatography on silica eluting with 0-5% MeOH in DCM afforded the title compound as a colourless oil;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883819B2
Source datasetuspto-grants-2014_11
ORD IDord-659cfae49486445b9d1d6b9b982ae3ba
Source noteuspto-grants-2014_11