Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzophenone | HCID 3102 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 118324254 | HCID 118324254 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 118324209 | HCID 118324209 | 44% |
Reaction Steps
To a suspension of 26 (8 mg, 0.028 mmol) and benzophenone (10.2 mg, 0.056 mmol) in a mixture of toluene (1 mL) and DME (1 mL) was added potassium tert-butoxide (18 mg, 0.16 mmol) at room temperature. The resulting reaction mixture was heated at 85° C. for 8 hours and then the solvent was evaporated under reduced pressure to obtain the crude reaction mixture, which was purified by column chromatography on silica gel using [CH2Cl2/MeOH (95:5)→CH2Cl2/MeOH (90:10)] as eluent to provide 4 (3.5 mg, 0.012 mmol, 44%) as a white solid along with unreacted starting material 26 (4 mg, 0.014 mmol, 53%). The physical and spectral properties of 4 were matched with those given in the literature.7
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09126965B1 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-4c41ba7b83c840839225174016268cf4 |
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| Source note | uspto-grants-2015_09 |
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