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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701662Generated: November 2, 2026

Hydroquinone → HCID 12570756, compound

https://huagongshe.com/reaction/1701662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroquinoneHCID 785—
ReactantSulfuric AcidHCID 1118—
ReactantAcrylic AcidHCID 6581—
Reactant1-Oxa-2-silacyclohexane, 2,2-dimethyl-HCID 79909—
SolventCyclohexaneHCID 8078—
ProductHCID 12570756HCID 12570756—

Reaction Conditions

Temperature100 °C

Reaction Steps

523.8 g. 1,1-dimethyl-1-sila-2-oxacyclohexane (4.0 moles), 304.7 g. acrylic acid (4.2 moles), 1.0 g. hydroquinone, 13.5 ml concentrated sulfuric acid, and 1200 ml cyclohexane are measured into a 3 liter reactor. The mixture is stirred during heating. The mixture is heated with steam (100° C.) and kept under dry air. Water formed during the reaction is removed continuously as the cyclohexane and water azeotrope. After 6 hrs. of heating, 31.9 ml water is collected and heating is stopped. The solution is then column filtered over 1 kg. activated alumina and filtered again over 740 g. grade 12 silica gel. The cyclohexane is removed from the product by rotary evaporation at reduced pressure. 1,3-bis (4-acryloxy butyl) tetramethyl disiloxane is obtained. The product is 98.3% pure by gas chromatography. The identity of the product is confirmed by infrared spectrum and elemental analysis. The analysis results are 55.96% C, 9.26% H, and 13.85% Si.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04195030
Source datasetuspto-grants-1980_03
ORD IDord-1c2b800b7ac64685aed2f0ffcc36b76a
Source noteuspto-grants-1980_03