Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diphenylacetylene | HCID 10390 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Dibenzyl | HCID 7647 | 0.4% |
| Product | cis-Stilbene | HCID 5356785 | 91% |
Reaction Steps
To the solution of one equivalent of TiCl4 (1.1 ml, 10 mmol) and 0.5 equivalent of diphenylacetylene (0.89g, 5 mmol) in THF (40 ml) at −78° C. 2 equivalents of n-butyllithium (12.5 ml, 20 mmol, 1.6M solution in hexane) was slowly added and the resulting red-brown reaction mixture stirred at −78° C. for 1 h. The reaction mixture was then allowed to warm up to room temperature over 0.5 h followed by hydrolysis with 20 ml of H2O. Extraction of the organic products was accomplished with ether anhydrous ether. cis-Stilbene (91%) and bibenzyl (0.4%) were obtained as the products.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06743872B1 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-d67bda8ade0d4492bd4b4a67d4973573 |
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| Source note | uspto-grants-2004_06 |
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