HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 4-(4-Bromophenoxy)cyclohexanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(4-Bromophenoxy)cyclohexanone | HCID 67248883 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(4-Bromophenoxy)cyclohexanol | HCID 67249674 | 72% |
Reaction Steps
Sodium borohydride (77.3 mg, 2.04 mmol) was added to a solution of 4-(4-bromophenoxy)cyclohexanone (500 mg, 1.86 mmol) in ethanol (10 mL) at room temperature. After 20 minutes the reaction was cooled to 00° C. and quenched by the addition of 1 N HCl (aq). The reaction was concentrated and the resulting residue was partitioned between ether and 1 N HCl (aq). The layers were separated, the organic layer was washed with water then dried (Na2SO4), filtered and concentrated. Purification on an Analogix SF15-12 g column (hexanes/ethyl acetate=8:2) afforded the title compound as a white solid (360 mg, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09180123B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-c04ad4b26c8240ef8feb0cef81da6354 |
| Source note | uspto-grants-2015_11 |