Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242883Generated: October 27, 2026

Tetrabutylammonium borohydride → HCID 68157561, compound

https://huagongshe.com/reaction/242883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium borohydrideHCID 169536—
ReactantHCID 13024711HCID 13024711—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68157561HCID 6815756198%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-40e5e02974344c31ba241808278df7e9
Source noteuspto-grants-2014_02