HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chromanone → Chroman-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chromanone | HCID 68110 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Chroman-4-ol | HCID 92890 | 956.5% |
Reaction Steps
To a MeOH (250 ml) solution of 4-chromanone (16.6 g, 11 mmol), at 0° C., was added NaBH4 (5.5 g, 145 mmol) in 1 g portions over a 30 min. period. After complete addition the mixture was stirred for 1 h with spontaneous warming. The reaction was quenched with the slow addition of aq. NH4Cl (100 ml). The MeOH was removed in vacuo and the residue extracted with Et2O (2×100 ml). The organic layers were dried over MgSO4 and treated with activated carbon. After filtration the Et2O was removed in vacuo to yield 15.8 g of chroman-4-ol as a clear oil. HRMS (ESI+) calcd for C9H10O2 m/z 150.0681 (M+H)+. Found 150.0679.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07244725B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-d5528d32fd1744f582aa011ee8dd4aba |
| Source note | uspto-grants-2007_07 |