HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 1-(4-Chloro-3-(methylsulfonyl)phenyl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(4-Chloro-3-(methylsulfonyl)phenyl)ethanone | HCID 58188228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-Chloro-3-(methylsulfonyl)phenyl)ethanol | HCID 58187981 | — |
Reaction Steps
A round bottom flask was charged with 1-(4-chloro-3-(methylsulfonyl)phenyl)ethanone (12.0 g, 50.0 mmol) and tetrahydrofuran (100 mL) at 0° C. Sodium borohydride (3.7 g, 100 mmol) was added in portions and the reaction was stirred for 12 h at room temperature. The reaction was quenched with ice and extracted with MTBE. The organic solvents were removed under reduced pressure and the residue was purified by flash chromatography to get the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08946439B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-04c9c3ac5a06490b9bbfb2cb5b8cfa06 |
| Source note | uspto-grants-2015_02 |