HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 12318384, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(2,4-Diphenylpyrimidin-5-yl)ethan-1-one | HCID 12318382 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 12318384 | HCID 12318384 | — |
Reaction Steps
To a mixture of 41.1 g (0.15 mole) of 2,4 -diphenyl-5-pyrimidyl metyl ketone in 500 ml methanol stirred at 5°-10° was added over 20 minutes 11.4 g (0.30 mole) sodium borohydride. The resulting solution was stirred at 5°-10° for 30 minutes and then stirred at ambient temperatures for 2 hours. The solvents were removed in vacuo and the residue was partitioned between 500 ml CHCl3 and 500 ml water. The aqueous layer was extracted with two 500 ml portions of CHCl3. The combined CHCl3 extracts were washed with 250 ml water, dried (MgSO4), and concentrated to dryness in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03969355 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-57862b7e0324407d8bbb4185a06d477d |
| Source note | uspto-grants-1976_07 |