HuagongsheHuagongshe Chemistry Print Report · For research reference only
Durene → Benzene, 1,1'-butylidenebis-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Durene | HCID 7269 | — |
| Reactant | Triethoxysilane | HCID 13830 | — |
| Product | Benzene, 1,1'-butylidenebis- | HCID 69753 | — |
Reaction Steps
Triethoxisilane (compound 2, 0.6 mmol) instead of pentamethyldisiloxane was used for the same reaction to Example 14A. 1H-NMR analysis with durene as an internal standard material without isolation of products showed that (4,4-diphenylbuthyl) triethoxysilane (compound 3) was produced with the yield of 85%, and 1,1-diphenylbutane (compound 4) was produced with the yield of 6%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08318967B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-917aa428d7844a5aaa678c34858fb67e |
| Source note | uspto-grants-2012_11 |