HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 15790297, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloropyrimidine | HCID 74404 | — |
| Reactant | 2-(4-Chlorophenyl)-2-[(1,2,4-triazol-1-yl)methyl]hexan-1-ol | HCID 15766665 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 15790297 | HCID 15790297 | 102.8% |
Reaction Steps
To a flask was charged 0.15 g (0.0034 mole) of 60% sodium hydride, washed with 2×30 mL hexane, in 20 mL of tetrahydrofuran. While stirring at room temperature, 1.0 g (0.0034 mole) of 2-(4-chlorophenyl)-2-[(1,2,4-triazol-1yl)methyl]hexan-1-ol was added. The slurry was stirred at room temperature and 0.39 g of 2-chloropyrimidine (0.0034 mole) was added. The reaction was stirred overnight after which TLC using ethyl acetate indicated the reaction was complete. The product was isolated from ether after quenching and washing with water. After drying and removal of the solvent, 1.30 g (100% yield) of an oil resulted.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05358939 |
| Source dataset | uspto-grants-1994_10 |
| ORD ID | ord-890e1b19b7d14f099f1b9d5f8d56692b |
| Source note | uspto-grants-1994_10 |