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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244191Generated: October 30, 2026

Thionyl Chloride → 4'-(4-Fluoro-6-methyl-3-trifluoromethyl-1H-inden-2-yl)4-propylbicyclohexyl

https://huagongshe.com/reaction/1244191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantPotassium FluorideHCID 522689—
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant7-Fluoro-5-methyl-2-(4'-propylbicyclohexyl-4-yl)-indan-1-oneHCID 12020439—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
Product4'-(4-Fluoro-6-methyl-3-trifluoromethyl-1H-inden-2-yl)4-propylbicyclohexylHCID 12020442—

Reaction Conditions

Temperature0 °C

Reaction Steps

8.5 g (0.023 mol) of 7-fluoro-5-methyl-2-(4′-propylbicyclohexyl-4-yl)-indan-1-one are dissolved in 50 ml of-tetrahydrofuran and the solution is cooled down to 0° C. 3.7 ml (0.025 mol) of trifluoromethyltrimethylsilane are added. 0.1 ml of tetrabutylammonium fluoride (1 M solution in THF) are added. After the reaction has ended, the mixture is subjected to conventional workup, and then the product is taken up in 40 ml of methanol, 200 mg of potassium fluoride are added and the mixture is refluxed for 10 hours. The resulting carbinol is dissolved in 30 ml of pyridine and 1.7 ml (0.024 mol) of thionyl chloride are added dropwise. The mixture is stirred for 10 hours at room temperature and then subjected to conventional workup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07122228B2
Source datasetuspto-grants-2006_10
ORD IDord-0939614006f744c5abe2b68dd2e3198d
Source noteuspto-grants-2006_10