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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014150Generated: October 30, 2026

Triethylamine → 1-[tert-Butyl(dimethyl)silyl]-3-methylpyrrolidin-2-one

https://huagongshe.com/reaction/1014150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-DimethylaminopyridineHCID 21885—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant3-Methylpyrrolidin-2-oneHCID 102848—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-[tert-Butyl(dimethyl)silyl]-3-methylpyrrolidin-2-oneHCID 5787810088.2%

Reaction Conditions

Temperature20 °C

Reaction Steps

In an oven-dried 500 ml flask under argon was dissolved 3-methyl-2-pyrrolidinone (0.186 mol, 18.4 g) in 200 ml methylene chloride. To this solution was added Triethylamine (0.223 mol, 22.6 g), Dimethylaminopyridine (0.019 mol, 2.27 g), and t-Butyldimethylsilyl chloride (0.204 mol, 30.8 g). This mixture was stirred for 18 hrs at 20° C. after which time it was poured into 500 ml water, the organic layer separated, washed with water (2×100 ml), brine (100 ml), dried with MgSO4 and concentrated. Resulting crude oil was purified on 400 g silica (EtOAc/Hexanes) yielding 35.0 g (88%) of 1-[(1,1-dimethylethyl)(dimethyl)silyl]-3-methyl-2-pyrrolidinone a clear oil. LCMS (ESI+)=214 m/z (MH+). 1H NMR (400 MHz, CDCl3) δ 3.40-3.25 (m, 2H), 2.50-2.40 (m, 1H), 2.30-2.20 (m, 1H), 1.70-1.60 (m, 1H), 1.20-1.18 (d, 3H, J=7.06 Hz), 0.95 (s, 9H), 0.29-0.27 (d, 6H, J=6.70 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07982053B2
Source datasetuspto-grants-2011_07
ORD IDord-47f7adb98446461db3c142920ea9f881
Source noteuspto-grants-2011_07