HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium borohydride → HCID 68157561, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium borohydride | HCID 169536 | — |
| Reactant | HCID 13024711 | HCID 13024711 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68157561 | HCID 68157561 | 98% |
Reaction Steps
Tetrabutylammonium borohydride (750 mg, 2.91 mmol) was added to a solution of 1-(3-phenylbenzofuran-2-yl)ethanone (459 mg, 1.94 mmol) in THF (9 mL) and IMS (1 mL) and the mixture stirred at RT for 1 h. The reaction mixture was quenched by addition of MeOH and volatiles were removed in vacuo. The resulting residue was purified by column chromatography (Si—PCC, gradient 0-40% EtOAc in cyclohexane) affording the title compound as an oil (452 mg, 98%). LCMS (Method C): RT 3.57 min [M-OH]+ 221.1
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653089B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-40e5e02974344c31ba241808278df7e9 |
| Source note | uspto-grants-2014_02 |