HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-one → HCID 12150152, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-one | HCID 70556 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 12150151 | HCID 12150151 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 12150152 | HCID 12150152 | — |
Reaction Steps
To a mixture of 4-(1,2,3,4-tetrahydro-1-naphthyloxy)benzaldehyde (264 mg, 1.05 mmol) and 1-phenyl-1,3,8-triazaspiro[4.5]decan-4-one (232 mg, 1.00 mmol) in 1,2-dichloroethane (15 mL) was added sodium triacetoxyborohydride (369 mg, 1.74 mmol). The resultant reaction mixture was stirred at room temperature under argon atmosphere for 20 h. The reaction mixture was quenched with 1 N aqueous NaHCO3 and extracted with CHCl3 (2×50 mL). The organic phase was dried over Na2SO4, filtered and concentrated. The crude product was purified by flash chromatography on silica gel (4% MeOH in CHCl3) to yield the title product as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06777421B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-726b7b831ff84896a4bdc7e072a3848e |
| Source note | uspto-grants-2004_08 |