HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium aluminum hydride → 2-ethyl-5-(4-fluoro-benzylamino)-2H-pyrazole-3-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium aluminum hydride | HCID 28112 | — |
| Reactant | Sodium sulfate decahydrate | HCID 62649 | — |
| Reactant | 2-ethyl-5-(4-fluoro-benzylamino)-2H-pyrazole-3-carboxylic acid methyl ester | HCID 57619383 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-ethyl-5-(4-fluoro-benzylamino)-2H-pyrazole-3-carbaldehyde | HCID 57619207 | — |
Reaction Steps
To 2-ethyl-5-(4-fluoro-benzylamino)-2H-pyrazole-3-carboxylic acid methyl ester (529, 1.00 g, 3.61 mol) in tetrahydrofuran (70.0 mL) under an atmosphere of nitrogen at room temperature, lithium tetrahydroaluminate (1.00M of in tetrahydrofuran, 10.00 mL) was slowly added. The reaction was stirred at room temperature overnight, followed by slowly adding sodium sulfate decahydrate (15.0 g). After 2 hours, the reaction was filtered, concentrated and purified with silica gel column chromatography eluting with 20% to 100% ethyl acetate in hexane to give a yellow oil (530, 0.16 g, 18%). MS (ESI) [M+H+]+=248.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08722702B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-2ec8cc02916049519ebe2b8aa35242ce |
| Source note | uspto-grants-2014_05 |