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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549354Generated: October 26, 2026

Acetonitrile → tert-butyl (2S)-2-(2-methoxy-2-oxoethyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/549354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantDiisopropylethylamineHCID 81531—
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant(S)-2-(1-BOC-2-pyrrolidinyl)acetic acidHCID 688605—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Producttert-butyl (2S)-2-(2-methoxy-2-oxoethyl)pyrrolidine-1-carboxylateHCID 11075654—

Reaction Steps

A solution of (S)-2-carboxymethyl-pyrrolidine-1-carboxylic acid tert-butyl ester (2.00 g) in methanol (1.32 ml)/acetonitrile (40 ml) was treated with N,N-diisopropylethylamine (1.78 ml). Trimethylsilyldiazomethane (2M, 8.73 ml) was added dropwise and the resulting mixture was stirred at room temperature, under argon for 24 h. The mixture was diluted with ethyl acetate, washed with 2M HCl, saturated aqueous sodium hydrogen carbonate, brine then dried (magnesium sulfate). The solvent was removed under reduced pressure to afford the title compound (2.10 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943645B2
Source datasetuspto-grants-2011_05
ORD IDord-67ba47f2c0724598a71ab82276e2df3f
Source noteuspto-grants-2011_05