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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242854Generated: October 27, 2026

Tetrabutylammonium borohydride → HCID 68157561, compound

https://huagongshe.com/reaction/242854

Reaction equation

Participants

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

Reaction Steps

Tetrabutylammonium borohydride (nBu4NBH4) (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 was stirred at RT for 1 h. The reaction mixture was then quenched by addition of MeOH and volatiles were removed under reduced pressure. The resulting residue was purified by column chromatography (Si—PCC, gradient 0-40% EtOAc in cyclohexane) affording 1-(3-phenylbenzofuran-2-yl)ethanol as an oil (452 mg, 98%). LCMS: 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-71c851395b0943c8a6242f69632e8bd1
Source noteuspto-grants-2014_02