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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420759Generated: October 25, 2026

Lithium iodide → 6-(2-hydroxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyran

https://huagongshe.com/reaction/1420759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium iodideHCID 66321—
Reactant6-(2-methoxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyranHCID 18782865—
SolventDichloromethaneHCID 6344—
Solvent2,4,6-TrimethylpyridineHCID 7953—
Product6-(2-hydroxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyranHCID 1878288835.9%

Reaction Conditions

Temperature150 °C

Reaction Steps

6-(2-Methoxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyran (3.5 g) (see Preparation 7) was dissolved in dry 2,4,6-collidine (15 ml), anhydrous lithium iodide (9.0 g) was added and the mixture was heated at 150° C for 40 hours. After cooling, the mixture was taken up in dichloromethane and washed with 2N aqueous hydrochloric acid solution (×3). The organic layer was dried (anhydrous sodium sulphate), the solvent removed under reduced pressure and the residue was chromatographed on silica using 1:1 hexane:dichloromethane as the eluent to yield 6-(2-hydroxyphenyl)thio-2,2,3-trimethyl-2H-benzo[b]pyran (1.2 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071938
Source datasetuspto-grants-2000_06
ORD IDord-c2d9dbbdab2c46f6814021f0ef5c1049
Source noteuspto-grants-2000_06