HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 178498838, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 19698828 | HCID 19698828 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178498838 | HCID 178498838 | 122.6% |
Reaction Steps
0.170 g (3 eq) of sodium borohydride is added to 0.400 g of 1-methyl-2-veratrylamino-5-methoxycarbonylpyrimidinium hydroxide dissolved in 50 ml of ethanol. The mixture is stirred under argon at room temperature for three hours. After evaporation of the ethanol, the medium is extracted with dichloromethane and water. The organic phases are washed with a saturated sodium chloride solution and then dried over sodium sulfate. The oil resulting from evaporation of the organic phases, purified on silica gel under medium pressure (eluent: 15% MeOH/CH2Cl2) gives 467 mg (yield: 98%) of the corresponding 1,6-dihydropyrimidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05480884 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-442fd9acca7948e98d873fc98cd9997a |
| Source note | uspto-grants-1996_01 |