Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Chloromethyl 2-(trimethylsilyl)ethyl ether | HCID 2724271 | — |
| Reactant | HCID 178520025 | HCID 178520025 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22486277 | HCID 22486277 | — |
Reaction Steps
The synthesis was performed with reference to the known literature (Tetrahedron, Vol. 63, p. 419, 2007). A solution of 1H-indazole-3-carboxaldehyde (0.888 g, 6.08 mmol) in methylene chloride (8 mL) was added with 50% aqueous potassium hydroxide (6 mL) and tetrabutylammonium bromide (0.0196 g, 0.0608 mmol), and the mixture was cooled on ice. The reaction mixture was added dropwise with 2-(trimethylsilyl)ethoxymethyl chloride (1.18 mL, 6.67 mmol), and the mixture was stirred for 1 hour under ice cooling, and then at room temperature overnight. The reaction mixture was added with water (30 mL), and the mixture was extracted three times with methylene chloride. The organic layer was dried over magnesium sulfate, and concentrated, and the resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain N-{[2-(trimethylsilyl)ethoxy]methyl}-1H-indazole-3-carboxaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09156827B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-cde0b90c9f854dddaef6bb1e20a989e7 |
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| Source note | uspto-grants-2015_10 |
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