HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 19702786, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 54086367 | HCID 54086367 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19702786 | HCID 19702786 | — |
Reaction Steps
To a solution of 63 mg of (4-ethylpyrimidin-5-yl)-4-methylpyrimidin-5-yl ketone in 1 ml EtOH chilled in an ice bath was added 7.4 mg of sodium borohydride. After stirring the solution for 30 minutes, 1 ml of EtOAc was added followed by 1 ml NaH2PO4 (pH=3.0). The mixture was stirred vigorously and the aqueous extracted with EtOAc (3 times). The organic layers were combined, dried (MgSO4) and filtered through silica gel with EtOAc. The solvent was evaporated to yield 52 mg of pure 1-(4-ethylpyrimidin-5-yl)-1-(4-methylpyrimidin-5-yl)methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05714438 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-d71a37ef3a754580a32349b2578dba7e |
| Source note | uspto-grants-1998_02 |