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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836554Generated: October 30, 2026

Triethylsilane → (4-{4-(Benzyloxy)-3-[(4-fluorophenyl)sulphonyl]benzyl}-3,5-dimethylphenoxy)(triisopropyl)silane

https://huagongshe.com/reaction/1836554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylsilyl triflateHCID 65367—
Reactant{4-(Benzyloxy)-3-[(4-fluorophenyl)sulphonyl]phenyl}{2,6-dimethyl-4-[(triisopropylsilyl)oxy]phenyl}methanolHCID 23499595—
SolventTetrahydrofuranHCID 8028—
Product(4-{4-(Benzyloxy)-3-[(4-fluorophenyl)sulphonyl]benzyl}-3,5-dimethylphenoxy)(triisopropyl)silaneHCID 23499604—

Reaction Steps

575 mg (0.89 mmol) of {4-(benzyloxy)-3-[(4-fluorophenyl)sulphonyl]phenyl}{2,6-dimethyl-4-[(triisopropylsilyl)oxy]phenyl}methanol (Example VIII) are dissolved in 10 ml of tetrahydrofuran. At 0° C., 1030.35 mg (8.86 mmol) of triethylsilane are initially added, and 78.78 mg (0.35 mmol) of trimethylsilyl trifluoromethane-sulphonate are then added dropwise. The reaction mixture is stirred for 1.5 hours, and saturated ammonium chloride solution is then added. The mixture is extracted three times with ethyl acetate, the combined organic phases are dried over sodium sulphate and the solvent is removed under reduced pressure. This gives 611 mg (53% of theory) of (4-{4-(benzyloxy)-3-[(4-fluorophenyl)sulphonyl]benzyl}-3,5-dimethylphenoxy)(triisopropyl)silane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777442B2
Source datasetuspto-grants-2004_08
ORD IDord-cf21c4ac4f5f41409caa839dd7674093
Source noteuspto-grants-2004_08