Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 131729268 | HCID 131729268 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131729269 | HCID 131729269 | 6% |
Reaction Steps
Firstly, dist. toluene (5 mL) was added to and dissolved in 1-(diallylethoxysilyl)-4-(3,5-dimethyl-3-hydroxy-hexynyl)benzene (125 mg, 0.35 mmol) obtained in Synthesis example 10. The resultant mixture was added with NaOH (9.9 mg, 0.25 mmol), and then was stirred under a nitrogen atmosphere at 80° C. for 16 hours to obtain a reaction mixture. Then, the reaction mixture was diluted with CH2Cl2, and an organic layer was washed with dist. H2O and sat. NaCl. The organic layer thus collected was dried with MgSO4, and the dried organic layer was filtered and concentrated to obtain a crude product. The obtained crude product was separated and purified by silica gel column chromatography (hexane/EtOAc=5/1) to obtain 1-(diallylethoxysilyl)-4-ethynylbenzene (5 mg, 6% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08053588B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-b5e00d7f33c646e7a88cc0beb97ee03f |
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| Source note | uspto-grants-2011_11 |
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