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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844744Generated: October 30, 2026

[4-(1-Ethoxycyclopropyl)-3-tert-butyl-phenoxy]-triisopropyl-silane → HCID 22568834, compound

https://huagongshe.com/reaction/844744

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[4-(1-Ethoxycyclopropyl)-3-tert-butyl-phenoxy]-triisopropyl-silaneHCID 22568790—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22568834HCID 22568834110.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of [4-(1-ethoxycyclopropyl)-3-tert-butyl-phenoxy]-triisopropyl-silane (Intermediate 108, 600.0 mg, 1.54 mmol) in 3 mL THF at 0° C. was added tetra,butylammonium fluoride (802.8.0 mg, 3.07 mmols; 3.1 mL of a 1 M solution in THF). The solution was stirred at 0° C. for 30 minutes and then quenched by the addition of H2O. The mixture was extracted with EtOAc and the combined organic layers were washed with H2O and saturated aqueous NaCl before being dried (MgSO4) and concentrated under reduced pressure. The title compound (400 mg, 88%) was isolated from the residue by column chromatography (4-10% EtOAc-hexanes) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380256B1
Source datasetuspto-grants-2002_04
ORD IDord-c6b2a4f4941143e98059ac353ea636de
Source noteuspto-grants-2002_04