HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 67630337, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | HCID 19702786 | HCID 19702786 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67630337 | HCID 67630337 | 86.5% |
Reaction Steps
To 3.2 mg of oil-free NaH was added 26 mg of 1-(4-ethylpyrimidin-5-yl)-1-(4-methylpyrimidin-5-yl)methanol in 1 ml THF at -30° C., followed by addition of 15 mg of pivaloyl chloride. After warming to room temperature and stirring for 1.5 hours, the reaction was quenched with 1 ml H2O and extracted with ether (3 times). The combined organics were washed with brine, dried (MgSO4) and evaporated to yield 30.7 mg of 1-(4-ethylpyrimidin-5-yl)-1-(4-methylpyrimidin-5-yl)-1-trimethylacetoxymethane as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05714438 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-a937adffbee2430d81874daede16fc3b |
| Source note | uspto-grants-1998_02 |