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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509284Generated: October 30, 2026

Ammonium Chloride → 8-(Trifluoromethyl)-1,4-dioxaspiro[4.5]decan-8-ol

https://huagongshe.com/reaction/509284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
ReactantTetrabutylammonium FluorideHCID 2724141—
SolventTetrahydrofuranHCID 8028—
Product8-(Trifluoromethyl)-1,4-dioxaspiro[4.5]decan-8-olHCID 6164525697%

Reaction Steps

1,4-cyclohexandione mono-ethylene ketal (1.5 g, 9.6 mmol) was dissolved in THF (35 ml), followed by sequential addition of trimethyl(trifluoromethyl)silane (2.8 ml, 19.2 mmol) and tetrabutylammonium fluoride (1.0M solution in THF, 20 ml, 20.0 mmol) at 0° C., and then the resulting mixture was stirred at room temperature for 2 hours. A saturated aqueous ammonium chloride solution (10 ml) was added to the resulting reaction liquid, and then, the resulting mixture was stirred for 10 minutes, followed by concentration under reduced pressure. Distilled water (10 ml) was added to the residue thus obtained, followed by extraction with MC (50 ml×2). The organic layer was dried over anhydrous sodium sulfate, followed by filtration and concentration, and then the residue thus obtained was subjected to MPLC (40% EtOAc/Hexanes), to obtain 2.1 g of yellow oil (97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096571B2
Source datasetuspto-grants-2015_08
ORD IDord-074953bd5b164d4c9d1a4c6fb4ad5f30
Source noteuspto-grants-2015_08