HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220033Generated: October 30, 2026
Tetrabutylammonium Fluoride → [(3-Hydroxyphenyl)(2-phenoxyethoxy)methylene]adamantane
https://huagongshe.com/reaction/2220033
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | [(3-tert-Butyldimethylsiloxyphenyl)(2-phenoxyethoxy)methylene]adamantane | HCID 23391581 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [(3-Hydroxyphenyl)(2-phenoxyethoxy)methylene]adamantane | HCID 18415643 | — |
Reaction Steps
To a solution of 6.30 parts of alkene (55) in 100 mL of THF was added 7.0 parts of 70% mixture of tetra-n-butylammonium fluoride in 50 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 300 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 3.75 parts. The structure of the product was confirmed on the basis of 1H NMR. The reaction proceeded as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07416898B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-a683d715f8354b72a10e6a40bec49f76 |
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| Source note | uspto-grants-2008_08 |
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