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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069539Generated: October 30, 2026

HCID 86649678, compound → ethyl 5-trimethylsilyl-1H-indole-2-carboxylate

https://huagongshe.com/reaction/2069539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86649678HCID 86649678—
CatalystRhodium(II) perfluorobutyrate dimerHCID 10942126—
SolventTolueneHCID 1140—
Productethyl 5-trimethylsilyl-1H-indole-2-carboxylateHCID 6684584256.4%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 1.7 g (5.90 mmol) of ethyl 2-azido-3-(3-trimethylsilylphenyl)propenoate prepared according to the procedure described in the preceding step, in 25 mL of dry toluene, maintained under an inert atmosphere, is added 0.62 g (0.59 mmol) of dirhodium (II) heptafluorobutyrate dimer complex. The reaction mixture is stirred for 7 hours at 40° C. A second portion of 0.62 g (0.59 mmol) of dirhodium (II) heptafluorobutyrate dimer complex is added to the reaction mixture while maintaining the stirring and heating at 40° C. for a further 1 hour. After cooling to room temperature, the reaction mixture is filtered through silica gel, eluting with toluene. The filtrate is then concentrated under reduced pressure. The greenish solid obtained is triturated several times in a minimum amount of heptane, until a white powder is obtained. This powder is dried under reduced pressure to give 0.87 g of the expected ethyl 5-trimethylsilyl-1H-indole-2-carboxylate in the form of a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299114B2
Source datasetuspto-grants-2012_10
ORD IDord-bca8f73f7e614fbca7a6df27c15e8366
Source noteuspto-grants-2012_10