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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586824Generated: November 1, 2026

Tetrahydrofuran → HCID 19759295, compound

https://huagongshe.com/reaction/1586824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantBenzo[b]thiophene, 2-(4-methylphenyl)-HCID 4137393—
ReactantButyllithiumHCID 178418339—
SolventDimethylformamideHCID 6228—
ProductHCID 19759295HCID 19759295—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 2-(4-methylphenyl)benzo[b]thiophene (896 mg) in freshly distillated tetrahydrofuran (15 ml) was added n-butyllithium (2.75 ml, 1.6 mol solution in n-hexane) through a syringe at -78° C. The solution was stirred at -78° C. for 10 minutes and then at ambient temperature for half an hour. To the deep red colored solution was added N,N-dimethylformamide (365mg) at 5° C. The mixture was stirred at ambient temperature for one hour, quenched with aqueous saturated ammonium chloride solution, and extracted with diethyl ether. The organic layer was washed with aqueous saturated ammonium chloride solution, dried, and concentrated in vacuo to give a yellow residue, which was purified by flash column chromatography on silica gel eluted with 50% n-hexane in dichloromethane to yield 2-(4-methylphenyl)benzo[b]thiophene-3-carbaldehyde (285 mg) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05215994
Source datasetuspto-grants-1993_06
ORD IDord-19ab70f4917b4ca7a518ef753b060680
Source noteuspto-grants-1993_06