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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594833Generated: October 27, 2026

Water → Ditert-butyl (2S,5S)-5-vinylpyrrolidine-1,2-dicarboxylate

https://huagongshe.com/reaction/594833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium Sodium TartrateHCID 9357—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant(S)-di-tert-butyl-5-formylpyrrolidine-1,2-dicarboxylateHCID 131734565—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductDitert-butyl (2S,5S)-5-vinylpyrrolidine-1,2-dicarboxylateHCID 6817111088%

Reaction Steps

93.5 ml (61.69 mmol, 2.0 eq) of a solution of KHMDS in toluene (15 w %, ABCR) was added under argon at RT to a suspension of 22.037 g (61.69 mmol, 2.0 eq) Ph3PMeBr in 220 ml THF, and the substance was stirred for 1 h. Then, a solution of 9.234 g (30.88 mmol, 1.0 eq) of the aldehyde 111 in 70 ml THF was dropped in at −78° C., and the resulting solution was stirred for 2.5 h at RT. 160 ml saturated Rochelle salt solution and 100 ml water was added to the reaction mixture, then extracted 3× with 260 ml MTBE each, the combined organic phases were washed with saturated NaCl solution and dried over magnesium sulfate. The solvent was removed at reduced pressure and, after purification by means of column chromatography on silica gel with EtOAc/CyHex (1:9) as eluent, 8.091 g (27.21 mmol, 88%) of the vinyl proline 112 was obtained as an isomeric mixture (d.r.: 1.7:1 cis:trans).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242985B2
Source datasetuspto-grants-2016_01
ORD IDord-24f97eae61c74fa19714a15f56a4e18b
Source noteuspto-grants-2016_01