HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 90389980, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(2-Phenyl-chroman-6-yloxy)-cyclohexanone | HCID 90390155 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 90389980 | HCID 90389980 | 96.3% |
Reaction Steps
500 mg of 4-(2-phenyl-chroman-6-yloxy)-cyclohexanone (1.6 mmol) were dissolved at 0° C. in 2.5 ml of ethanol. 30 mg of sodium borohydride (0.78 mmol) were added in portions, and stirring at room temperature was continued for 2 h. The solvent was removed under reduced pressure and the residue separated between saturated aqueous sodium hydrogencarbonate solution and dichloromethane. The aqueous layer was extracted with dichloromethane. The combined organic layers were dried with sodium sulfate and filtered, and volatile components removed under reduced pressure. 500 mg of the title compound were obtained as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09440941B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-bad77bf8f38c4ed28ed07e45a81f81f7 |
| Source note | uspto-grants-2016_09 |