Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748962Generated: October 30, 2026

Hydrochloric Acid → 6-Methoxy-2-[4-(methylsulfanyl)phenyl]naphthalen-1-ol

https://huagongshe.com/reaction/748962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant6-Methoxy-alpha-tetraloneHCID 14112—
Reactant4-BromothioanisoleHCID 66037—
Reactant2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product6-Methoxy-2-[4-(methylsulfanyl)phenyl]naphthalen-1-olHCID 68518817—

Reaction Steps

Place 6-methoxy-1-tetralone (1 eq.), 4-bromothioanisole (2.5 eq.), palladium acetate (0.01 eq.), 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl (0.02 eq.) and toluene in a 3 neck flask equipped with a mechanical stirrer, reflux condenser, nitrogen purge and a temperature probe. Add sodium tert-butoxide (4 eq.) and heat the slurry to reflux. After about 2-4 hours, cool the reaction to room temperature and add 3M aqueous HCl along with tetrahydrofuran. Stir the biphasic reaction mixture for 30 minutes before filtration and separation of the layers. Concentrate the organic layer to isolate 6-methoxy-2-(4-methylthiophenyl)naphthalene-1-ol by filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399867B2
Source datasetuspto-grants-2008_07
ORD IDord-ae155ea000984dd195ac0aaddec3f248
Source noteuspto-grants-2008_07