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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216252Generated: October 31, 2026

Ethyl trimethylsilylacetate → HCID 21941242, compound

https://huagongshe.com/reaction/2216252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl trimethylsilylacetateHCID 77687—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantHCID 21941240HCID 21941240—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystTolueneHCID 1140—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 21941242HCID 21941242126.9%

Reaction Conditions

Temperature90 °C

Reaction Steps

5-Bromo-2-(2-methylpropyl)indazole (1.41 g, 0.0056 mol) and palladium acetate (0.063 g, 0.00028 mol) were stirred in toluene (10 ml) under an atmosphere of nitrogen. Ethyl trimethylsilylacetate (2.35 ml, 0.0115 mol), potassium tert-butoxide (0.66 g, 0.059 mol) and a 10% w/v solution of tri-tert-butylphosphine in toluene (0.97 ml, 0.00048 mol) were added sequentially and then the mixture was heated to 90° C. for 105 minutes. The mixture was cooled to room temperature, diluted with diethyl ether and filtered through diatomaceous earth and the filtrate was evaporated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with 2:1 diethyl ether:hexane to give ethyl[2-(2-methylpropyl)indazol-5-yl]acetate (1.85 g), as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112553B1
Source datasetuspto-grants-2006_09
ORD IDord-c42a42c0406b4ea293ec0e26aed7aaca
Source noteuspto-grants-2006_09