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 (1.00 M 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 | US09169250B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-18ea33246ef74549a503805d2487dc02 |
| Source note | uspto-grants-2015_10 |