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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504335Generated: October 31, 2026

Potassium Carbonate → (S,E)-1-tert-butyl 2-methyl 4-(methoxymethylene)pyrrolidine-1,2-dicarboxylate

https://huagongshe.com/reaction/1504335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-tert-butyl 2-methyl (2S)-4-oxopyrrolidine-1,2-dicarboxylateHCID 10988485—
Reactant(1E)-1-diazo-1-dimethoxyphosphorylpropan-2-oneHCID 136023029—
SolventMethanolHCID 887—
Product(S,E)-1-tert-butyl 2-methyl 4-(methoxymethylene)pyrrolidine-1,2-dicarboxylateHCID 866828103,057.4%

Reaction Steps

Potassium carbonate (200 g, 2.17 mmol) was added to a solution of (S)-1-tert-butyl 2-methyl 4-oxopyrrolidine-1,2-dicarboxylate (88 g, 362 mmol) and dimethyl 1-diazo-2-oxopropylphosphonate (200 g, 1.04 mol) in methanol (1 L) at 0° C. and the reaction mixture was stirred at RT overnight, quenched, concentrated, poured into water, extracted with DCM, and purified by column chromatography to provide the title intermediate (18 g, 17% yield) as a yellow oil. 1H NMR (400 MHz, CDCl3): δ(ppm) 1.406-1.457 (d, 9H, J=20.4 Hz), 2.502-2.520 (m, 1H), 2.601-2.631 (m, 1H), 2.720-2.782 (m, 1H), 3.578 (s, 3H), 3.707 (s, 3H), 3.952-3.983 (m, 1H), 4.302-4.375 (m, 1H), 4.471-4.490 (m, 1H), 5.810-5.968 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212168B2
Source datasetuspto-grants-2015_12
ORD IDord-e3281c51be3b4cfbb623095dafb78de6
Source noteuspto-grants-2015_12