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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822079Generated: November 1, 2026

Tetraethoxysilane → HCID 57894271, compound

https://huagongshe.com/reaction/1822079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetraethoxysilaneHCID 6517—
ReactantTetrahydrofuranHCID 8028—
Reactantp-DiiodobenzeneHCID 12208—
ReactantHCID 178418918HCID 178418918—
SolventDiethyl EtherHCID 3283—
ProductHCID 57894271HCID 5789427161%

Reaction Conditions

Temperature-30 °C

Reaction Steps

At first, a mixed solution of 1,4-diiodobenzene (15 g, 45.6 mmol) and a distilled tetrahydrofuran solution (dist.THF: 114 mL) was added dropwise with 2 mol/L of i-PrMgCl (24 mL (solvent: THF), 48 mmol) at −30° C. Then, the resultant mixture was stirred under a nitrogen atmosphere at −30° C. for 5.5 hours to obtain a reaction solution. Subsequently, the reaction solution was added dropwise (3 drops per second) using a cannula into a mixed solution of tetraethoxysilane (TEOS: 60.6 mL, 272 mmol) and dist.THF (90 mL), which was cooled to −30° C. Thereafter, the resultant mixed solution was stirred at −30° C. for one hour, and further stirred at room temperature for 44 hours to obtain a reaction mixture. After that, the obtained reaction mixture was added with ether (100 ml), and washed with distilled water (dist.H2O). Then, the aqueous layer was extracted with ether. The collected organic layers were washed with sat.NaCl, dried with MgSO4), filtered and concentrated to obtain a crude product. Thereafter, the crude product thus obtained was purified by distillation under a reduced pressure (1.5 mmHg, 120° C.), and thereby 4-(triethoxysilyl)iodobenzene was obtained (10.2 g, 61% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608673B2
Source datasetuspto-grants-2009_10
ORD IDord-e6e45745733d4dd8b9fb4f6d69c75eb0
Source noteuspto-grants-2009_10