HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216252Generated: October 31, 2026
Ethyl trimethylsilylacetate → HCID 21941242, compound
https://huagongshe.com/reaction/2216252
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl trimethylsilylacetate | HCID 77687 | — |
| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | HCID 21941240 | HCID 21941240 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | Toluene | HCID 1140 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 21941242 | HCID 21941242 | 126.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07112553B1 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-c42a42c0406b4ea293ec0e26aed7aaca |
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| Source note | uspto-grants-2006_09 |
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