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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900765Generated: October 29, 2026

Tetrahydrofuran → Phenyl(8-thiabicyclo[3.2.1]oct-3-yl)methanone

https://huagongshe.com/reaction/900765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant8-Thiabicyclo[3.2.1]octane-3-carbonitrileHCID 69290896—
ReactantHCID 178418255HCID 178418255—
ProductPhenyl(8-thiabicyclo[3.2.1]oct-3-yl)methanoneHCID 6929082238%

Reaction Steps

A 3M etheral solution of phenyl magnesium bromide (6.72 ml, 20.16 mmol) was added at 0° C. to a solution of the above nitrile (1.03 g, 6.72 mmol) in dry THF (10 ml). After 30 minutes, the ice bath was removed and the reaction continued at room temperature for 16 hours. The reaction was carefully quenched by addition of a saturated aqueous NH4Cl solution. After addition of ether, organic layer was separated, washed with brine, dried over MgSO4 and concentrated. The residual oil was chromatographied on silica gel (hexane/AcOEt 94/6) to give the phenyl(8-thiabicyclo[3.2.1]oct-3-yl)methanone 22 as a colorless oil (586 mg, 38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361668B2
Source datasetuspto-grants-2008_04
ORD IDord-ee9570609fa24743980c2785cc4347bf
Source noteuspto-grants-2008_04