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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911249Generated: October 29, 2026

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

https://huagongshe.com/reaction/1911249

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 numberUS08604050B2
Source datasetuspto-grants-2013_12
ORD IDord-e5d7f90fd0d644cbb7a2ca288a869d98
Source noteuspto-grants-2013_12