HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 11391116, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(Tert-butyldimethylsilanyloxy)-1-phenylethanone | HCID 13523338 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 11391116 | HCID 11391116 | 29% |
Reaction Steps
To a solution of 2-(tert-butyldimethylsilanyloxy)-1-phenylethanone (2.5 g, 10 mmol, Example 4) in methanol (30 ml) added with sodium borohydride (378 mg, 10 mmol) at room temperature. The mixture was stirred at room temperature for 5.5 hours and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent; hexane/ethyl acetate=3/1) to give 2-(tert-butyldimethylsilanyloxy)-1-phenylethanol (0.73 g, 2.9 mmol, 29%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09006232B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-72cbc16cebb24932838bfa7841923826 |
| Source note | uspto-grants-2015_04 |