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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804747Generated: October 31, 2026

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

https://huagongshe.com/reaction/1804747

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 numberUS08354425B2
Source datasetuspto-grants-2013_01
ORD IDord-ed2427893f40451396d041bd4f301acc
Source noteuspto-grants-2013_01