Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Acrylic Acid | HCID 6581 | — |
| Reactant | 1-Oxa-2-silacyclohexane, 2,2-dimethyl- | HCID 79909 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 12570756 | HCID 12570756 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04195030 |
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| Source dataset | uspto-grants-1980_03 |
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| ORD ID | ord-1c2b800b7ac64685aed2f0ffcc36b76a |
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| Source note | uspto-grants-1980_03 |
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