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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512010Generated: October 30, 2026

Tetrahydrofuran → HCID 20099906, compound

https://huagongshe.com/reaction/512010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant3'-(Benzyloxy)[1,1'-biphenyl]-3-carbonitrileHCID 20099937—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventHexaneHCID 8058—
ProductHCID 20099906HCID 2009990675%

Reaction Steps

To a stirred solution of 75 (0.12 g, 0.42 mmol) in anhydrous THF (10 mL) at −78° C., under a nitrogen atmosphere was added diisobutylaluminum hydride (0.5 mL, 0-5 mmol, using a 1M solution in hexane) dropwise. The reaction mixture was stirred at the same temperature for 1 hour and then quenched by dropwise addition of potassium sodium tartrate (10% solution in water). The resulting mixture was warmed to room temperature, diluted with diethyl ether (20 mL) and stirred vigorously for 1 h. The organic phase was separated and the aqueous phase was extracted with diethyl ether. The combined organic layer was washed with brine, dried (MgSO4) and evaporated under reduced pressure. The residue obtained was purified by flash column chromatography on silica gel (20% diethyl ether-hexane) to give 76 (0.091 g, 75% yield) as a viscous liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102622B2
Source datasetuspto-grants-2015_08
ORD IDord-72901e627ee248cb8a1adc9e0e1f68c8
Source noteuspto-grants-2015_08