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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093269Generated: November 3, 2026

Tetraethoxysilane → HCID 131730584, compound

https://huagongshe.com/reaction/2093269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetraethoxysilaneHCID 6517—
Reactant3,4-DihydroxybenzaldehydeHCID 8768—
SolventTolueneHCID 1140—
ProductHCID 131730584HCID 131730584—

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 3,4-dihydroxybenzaldehyde (27.6 g, 200 mmol) and toluene (220 mL) was dehydrated by distilling 5 mL of the solution. Thereafter, 20.8 g (100 mmol) of tetraethoxysilane (TEOS) was added to the solution while stirring. The mixed solution was refluxed for 1 hour, and then, while the distillation temperature was 100° C. or higher, distilled until the amount of the solution became half. After the distillation, solid content of the product was isolated by suction filtering using a membrane suction filter. The residual solid content was heated to 100° C. under vacuum using a vacuum dryer so that remaining volatile components were completely removed. The solid content (3,4-dihydroxybenzaldehyde-silicon complex) was black in color. The yield amount was 30.0 g (100 mmol), and the yield percentage was 100%. 15 g of 3,4-dihydroxybenzaldehyde-silicon complex was dissolved into 100 mL of 1:9 dimethylsulfoxide/ethanol to produce a coating liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445118B2
Source datasetuspto-grants-2013_05
ORD IDord-2ce2ee875e8642029c311c9dbb01999e
Source noteuspto-grants-2013_05