Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363123Generated: November 1, 2026

Ammonium Chloride → HCID 58319265, compound

https://huagongshe.com/reaction/2363123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 67111134HCID 67111134—
SolventDiethyl EtherHCID 3283—
ProductHCID 58319265HCID 5831926579.4%

Reaction Steps

To a suspension of CH3PPh3I (664 mg, 1.64 mmol) in Et2O (20 mL) was added t-BuOK (184 mg, 1.64 mmol). The mixture was stirred for 15 minutes, to which was added dropwise 1-[3-(tert-butyl-dimethyl-silanyloxy)-5-trifluoromethyl-phenyl]-ethanone (436 mg, 1.37 mmol). The mixture was stirred at room temperature overnight and then diluted with Et2O. The mixture was filtered on a pad of celite. The residue compound was concentrated under reduced pressure. The crude residue was dissolved in THF and was added 1M-TBAF (in THF, 1.2 eq, 1.0M in CH2Cl2). The reaction mixture was stirred for 30 min at room temperature, treated with saturated ammonium chloride, and then extracted with EtOAc. The organic layer was dried over magnesium sulfate and concentrated in vacuo. The crude product was purified by column chromatography to give 3-isopropenyl-5-trifluoromethyl-phenol (220 mg, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691855B2
Source datasetuspto-grants-2014_04
ORD IDord-a90623b9769b484d8c850f5c24f95d46
Source noteuspto-grants-2014_04