HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → HCID 14590584, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178469928 | HCID 178469928 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 14590584 | HCID 14590584 | — |
Reaction Steps
To a solution of 3-amino-1H-pyrazole-4-carboxylic acid ethyl ester (5.0 g, 32 mmol) in acetonitrile is added sodium hydride (1.28 g, 32 mmol) at RT. After 30 min of stirring, a solution of ethyl iodide (2.57 ml, 32 mmol) in acetonitriloe is added dropwise. The reaction mixture is stirred at RT for 16 h. Water is added followed by anhydrous sodium sulfate. The mixture is filtered and concentrated at reduced pressure. The crude product is chromatographed on silica gel using 30% ethyl acetate in hexanes to provide a regioisomeric mixture of N-ethylated 3-amino-1H-pyrazole-4-carboxylic acid ethyl esters. This mixture is used in the following reaction step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538135B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-0be3875414ae4139b110bbd813c61961 |
| Source note | uspto-grants-2009_05 |