HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 43394335, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 59565074 | HCID 59565074 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 43394335 | HCID 43394335 | 100% |
Reaction Steps
NaBH4 (719 mg, 19.0 mmol) was added in portions to a suspension of 1-(4-(trifluoromethoxy)phenylsulfonyl)piperidin-4-one (3.07 g, 9.50 mmol) in ethanol (50 ml) at 0° C. and stirred at room temperature for 2 hours. The reaction was quenched with acetone (50 ml) at 0° C. and concentrated in vacuo. The residue was diluted with ethyl acetate (100 ml), washed with saturated aqueous NaHCO3 and brine, dried over Na2SO4, filtered and concentrated in vacuo to give 1-(4-(trifluoromethoxy)phenylsulfonyl)piperidin-4-ol (3.09 g, 100%) as a white solid: LCMS: 326 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08518934B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-a6654cbde3cb41839bf38c7ffb9c8b4a |
| Source note | uspto-grants-2013_08 |