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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253134Generated: October 30, 2026

Lithium tri-s-butylborohydride → HCID 11220647, compound

https://huagongshe.com/reaction/253134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium tri-s-butylborohydrideHCID 3611392—
ReactantHCID 86614018HCID 86614018—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11220647HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872009B2
Source datasetuspto-grants-2011_01
ORD IDord-607b9af0a888451f8b270417de50ad6b
Source noteuspto-grants-2011_01