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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484190Generated: November 2, 2026

1,3,5-Tribromobenzene → Silane, 1,3,5-benzenetriyltris[triethoxy-

https://huagongshe.com/reaction/484190

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3,5-TribromobenzeneHCID 12279—
ReactantCesium iodideHCID 24601—
Reactant1,3-Bis(triethoxysilyl)benzeneHCID 11603772—
ProductSilane, 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05229481
Source datasetuspto-grants-1993_07
ORD IDord-b6f21b4eb82f4acf8a3c32a05281af82
Source noteuspto-grants-1993_07