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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475335Generated: October 25, 2026

Trimethylsilyl iodide → methyl (5R)-5-((trimethylsilyl)ethynyl)-L-prolinate

https://huagongshe.com/reaction/475335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
Reactantdimethyl(2S,5R)-5-((trimethylsilyl)ethynyl)pyrrolidine-1,2-dicarboxylateHCID 11161884—
SolventChloroformHCID 6212—
Productmethyl (5R)-5-((trimethylsilyl)ethynyl)-L-prolinateHCID 16090847—

Reaction Steps

A solution of dimethyl(2S,5R)-5-((trimethylsilyl)ethynyl)pyrrolidine-1,2-dicarboxylate (5.43 g, 19.16 mmol) and iodotrimethylsilane (3 mL, 28.74 mmol) in chloroform (100 mL) was heated to 65° C. for 3 hours, was cooled to room temperature, concentrated under reduced pressure and flash chromatographed with 35% ethyl acetate/65% hexane to provide the titled compound. MS (DCI/NH3) m/e 226 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637546B2
Source datasetuspto-grants-2014_01
ORD IDord-536aa212691d4fbf9e505858ef135f9e
Source noteuspto-grants-2014_01