HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 1-(3-(Trifluoromethyl)phenylsulfonyl)piperidin-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(3-(Trifluoromethyl)phenylsulfonyl)piperidin-4-one | HCID 10709847 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(3-(Trifluoromethyl)phenylsulfonyl)piperidin-4-ol | HCID 3729262 | 84.1% |
Reaction Steps
NaBH4 (180 mg, 4.74 mmol) was added to a solution of 1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-4-one (2.56 g, 8.34 mmol) in methanol (15 ml) at 0° C., and stirred at room temperature for 1 hour. The reaction was quenched with H2O (50 ml) and extracted with ethyl acetate (20 ml×2). The combined organic phase was washed with H2O (20 ml×2) and brine (20 ml×2), dried over Na2SO4 and concentrated in vacuo to give 1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-4-ol (2.17 g, 84%) as a white solid: LCMS: 310 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08518934B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-b6fd2e18d3e54e1c939e1c9fa01842ae |
| Source note | uspto-grants-2013_08 |