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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420755Generated: October 26, 2026

3-Methoxybenzenethiol → 6-(3-methoxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyran

https://huagongshe.com/reaction/1420755

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxybenzenethiolHCID 84989—
Reactant6-Bromo-2,2,3-trimethyl-2H-benzo[b]pyranHCID 14956089—
ReactantSodium t-butoxideHCID 23676156—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
Product6-(3-methoxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyranHCID 1878287689.8%

Reaction Steps

6-Bromo-2,2,3-trimethyl-2H-benzo[b]pyran (6.5 g) (see Preparation 4) was dissolved in absolute ethanol (135 ml), then sodium tert-butoxide (7.5 g), 3-methoxybenzenethiol (3.6 g) and tetrakis(triphenylphosphine)palladium(0) (0.35 g) were added and the mixture was heated under reflux under a nitrogen atmosphere for 48 hours. Further tetrakis(triphenylphosphine)palladium(0) (0.3 g) was added and heating was continued for a further 48 hours. The solvent was removed under reduced pressure and the residue was dissolved in dichloromethane and washed with water. The organic layer was dried (anhydrous sodium sulphate), the solvent removed under reduced pressure and the crude product chromatographed on silica using 1:1 hexane:dichloromethane as the eluent to yield 6-(3-methoxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyran (7.2 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071938
Source datasetuspto-grants-2000_06
ORD IDord-efbe90a7f78546fcac0fa747596e88cc
Source noteuspto-grants-2000_06