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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898653Generated: October 29, 2026

Stannane, tributyl(1-ethoxyethenyl)- → 1-(3,4-dihydro-2H-1-benzopyran-6-yl)ethan-1-one

https://huagongshe.com/reaction/898653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
Reactant6-BromochromanHCID 10856814—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
Product1-(3,4-dihydro-2H-1-benzopyran-6-yl)ethan-1-oneHCID 12357018—

Reaction Steps

In accordance with this scheme a 6-bromochroman compound of Formula 2 (see Reaction Scheme 1) is reacted with by tributyl(1-ethoxyvinyl)tin in the presence dichlorobis(triphenylphosphine)palladium(II) under an inert gas (argon) atmosphere in an aprotic neutral solvent, such as tetrahydrofuran (THF), to provide a 6-acetylchroman derivative of Formula 25. The 6-acetylchroman derivative of Formula 25 is then reacted with iodine and silver(I)trifluoromethanesulfonate (AgOTf) to give a 6-acetyl-8-iodochroman derivative of Formula 26. The compound of Formula 26 is reacted with with trimethylsilyl acetylene in triethyl amine under argon atmosphere in the presence of copper(I)iodide and dichlorobis(triphenylphosphine)palladium(II) (Pd(PPh3)2Cl2) to give the 6-acetyl-8-trimethylsilanyl-ethynyl-chroman derivative of Formula 27. The latter reaction is analogous to the conversion of the 8-iodo-substituted chroman compounds of Formula 4 to the 8-trimethylsilanyl-ethynyl-chroman derivatives of Formula 5, as shown in Reaction Scheme 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351737B2
Source datasetuspto-grants-2008_04
ORD IDord-b54563c181444f5fb6f6bf78e478877c
Source noteuspto-grants-2008_04