HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414559Generated: October 30, 2026
Sodium borohydride → HCID 14373286, compound
https://huagongshe.com/reaction/414559
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 15123282 | HCID 15123282 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 14373286 | HCID 14373286 | — |
Reaction Steps
To a solution of 240 mg of 6-[1-hydroxy-1-phenyl(3-pyridyl)methyl]-3,4-dihydrocarbostyril in 5 ml of trifluoroacetic acid at 0° C. was added 280 mg of sodium borohydride. When hydrogen evolution ceased the mixture was stirred at 25° C. for 30 minutes, then the solvent was removed under reduced pressure. The residue was added to aqueous potassium carbonate solution and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, the solvent removed under reduced pressure and the residue chromatographed on silica gel, eluting with 3% methanol in methylene chloride to give 6-[phenyl(3-pyridyl)methyl]-3,4-dihydrocarbostyril, m.p. 95°-96° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04792561 |
|---|
| Source dataset | uspto-grants-1988_12 |
|---|
| ORD ID | ord-8836d1fcc9ba400ba06586397e462cdd |
|---|
| Source note | uspto-grants-1988_12 |
|---|