HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium tri-s-butylborohydride → HCID 11220647, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium tri-s-butylborohydride | HCID 3611392 | — |
| Reactant | HCID 86614018 | HCID 86614018 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11220647 | HCID 11220647 | — |
Reaction Steps
To (R)-benzyl 1-oxo-1-phenylpent-4-en-2-ylcarbamate (2.13 g, 6.89 mmol) in THF (50 mL) at −78° C. under argon was added lithium tri-sec-butylborohydride (20.7 ml, 20.7 mmol). Allowed the mixture to stir for 45 min. Quenched the reaction with saturated aqueous Rochelle's salt (50 mL) and the volatiles were removed in vacuo. The aqueous residue was extracted with ether (3×50 mL). The ether was combined and washed with brine (20 mL), dried over Na2SO4 and filtered. The filtrate was evaporated onto silica gel and purified via flash chromatography (0% to 20%; EtOAc in hexanes). MS m/z=334 [M+Na]+. Calc'd for C19H21NO3: 311.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07872009B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-607b9af0a888451f8b270417de50ad6b |
| Source note | uspto-grants-2011_01 |