HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3,5-Tribromobenzene → Silane, 1,3,5-benzenetriyltris[triethoxy-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3,5-Tribromobenzene | HCID 12279 | — |
| Reactant | Cesium iodide | HCID 24601 | — |
| Reactant | 1,3-Bis(triethoxysilyl)benzene | HCID 11603772 | — |
| Product | Silane, 1,3,5-benzenetriyltris[triethoxy- | HCID 11713854 | — |
Reaction Steps
The procedure used for the preparation of 1,3-di(triethoxysilyl)benzene was followed using 1,3,5-tribromobenzene (100.0 g, 0.318 mol) in place of 1,3-dibromobenzene. Two distillations gave a clear, colorless oil (0.1 mmHg, 196-198° C., 23.4 g, 13%). Anal. Calcd for C24H48O9Si3 : C, 51.0: H, 8.56. Found: C, 51.2; H, 8.53. IR (Neat, CsI, cm-1) : 2964 s, 2920 s, 2880 s, 2730 w, 1560 m, 1480 w, 1440 m, 1386 s, 1290 m, 1160 s, 1090 vs, 955 s, 825 s, 775 s, 710 m, 670 m, 487 s. 1H NMR (benzene -d6, 22° C., 300 MHz : δ 1.16 (t, J=7.1 Hz, 18 H, OCH2CH 3), 3.87 (q, J=7.1 Hz, 12 H, OCH2CH3, 8.55 (s, 1H, C6H4). 13C{1H} NMR (benzene-d6, 22° C., 75.5 MHz ): δ 18.43 (OCH2CH3), 58.92 (OCH2CH3), 130.83, 143.60 (C6H4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05229481 |
| Source dataset | uspto-grants-1993_07 |
| ORD ID | ord-b6f21b4eb82f4acf8a3c32a05281af82 |
| Source note | uspto-grants-1993_07 |