Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855872Generated: October 29, 2026

Tin tetrachloride → dimethyl(2S,5R)-5-propynyl-pyrrolidine-1,2-dicarboxylate

https://huagongshe.com/reaction/855872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTin tetrachlorideHCID 24287—
Reactant1-(Trimethylsilyl)prop-1-yneHCID 80363—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantDimethyl (2S)-5-methoxypyrrolidine-1,2-dicarboxylateHCID 11053097—
SolventDichloromethaneHCID 6344—
Productdimethyl(2S,5R)-5-propynyl-pyrrolidine-1,2-dicarboxylateHCID 66756906—

Reaction Steps

To a cold −45° C. solution of dimethyl(2S)-5-methoxypyrrolidine-1,2-dicarboxylate (10 g, 46.08 mmol, Example 1B) and trimethylsilylpropyne (14.24 ml, 92.16 mmol, 2.0 equiv) in methylene chloride (180 mL) was added a solution of tin (IV) chloride (1 M in methylene chloride, 60.0 mL, 60.0 mmol, 1.3 equiv) dropwise via an addition funnel over 30 minutes. To the dark yellow solution was added solid aluminum chloride (8.58 g, 64.52 mmol, 1.4 equiv) in one portion. The resulting mixture was allowed to warm to room temperature and stirred at room temperature for 48 hours. The reaction mixture was carefully quenched by saturated aqueous NH4OH (100 mL) with ice cooling. A white precipitate formed and was removed by filtration. The crude product was obtained after concentration. The residue was chromatographed on a Biotage flash 40 M eluting with 70% hexane/30% ethyl acetate to afford the titled compound. MS (DCI/NH3) m/e 226 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262207B2
Source datasetuspto-grants-2007_08
ORD IDord-2c027b7503a84042a10573410ddd4e96
Source noteuspto-grants-2007_08