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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220035Generated: October 27, 2026

Tetrabutylammonium Fluoride → [(3-Hydroxyphenyl)(2-phenoxyethoxy)methylene]-5-chloroadamantane

https://huagongshe.com/reaction/2220035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant[(3-tert-Butyldimethylsiloxyphenyl)(2-phenoxyethoxy)methylene]-5-chloroadamantaneHCID 23391585—
SolventTetrahydrofuranHCID 8028—
Product[(3-Hydroxyphenyl)(2-phenoxyethoxy)methylene]-5-chloroadamantaneHCID 18415644—

Reaction Steps

To a solution of 4.9 parts of alkene (64) in 75 mL of THF was added 5.0 parts of 70% mixture of tetra-n-butylammonium fluoride in 25 mL of THF over a period of 15 minutes. The reaction mixture was stirred for two hours. TLC on silica gel plate showed the formation of new product. The solvent was evaporated under reduced pressure and the oily material was dissolved in 150 mL of ethyl acetate and washed with two times with 200 mL of water. After drying over anhydrous sodium sulfate, the solvent was evaporated and the oily product was purified on silica gel column. TLC on silica gel plate of the fractions were checked and the combined organic solvent was evaporated, yield 2.5 parts. The structure of the product was confirmed on the basis of 1H NMR. The reaction proceeded as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07416898B2
Source datasetuspto-grants-2008_08
ORD IDord-0486319bd05542289f97394cb209447c
Source noteuspto-grants-2008_08