Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrabutylammonium Fluoride Trihydrate | HCID 11726816 | — |
| Reactant | HCID 14274478 | HCID 14274478 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14274479 | HCID 14274479 | 96.4% |
Reaction Steps
To a solution of 5.0 g (7 mmol) of diphenylbis(3,5-di-tert-butyl-4-trimethylsilyloxyphenyl)silane in 30 ml of tetrahydrofuran at 0° C. is added dropwise a solution of 4.3 g (14 mmol) of tetrabutylammonium fluoride trihydrate in 35 ml of tetrahydrofuran. The reaction mixture is stirred for 5 minutes at 0° C. and to it is added dropwise a solution of 2.2 g (62 mmol) of concentrated hydrochloric acid in 10 ml of tetrahydrofuran. The solvent is removed in vacuo and to the residue is added 250 ml of diethylether. The solution is extracted (3×100 ml) with water. The organic phase is dried over anhydrous sodium sulfate and the solvent is removed in vacuo to give 4.0 grams of a white solid. The crude product is recrystallized from heptane to give 3.0 g (75%) of product as white crystals; mp. 193°-194.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04783495 |
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| Source dataset | uspto-grants-1988_11 |
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| ORD ID | ord-3b053e224dc649d785b3923bc8bb0bc7 |
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| Source note | uspto-grants-1988_11 |
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