Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glycerol | HCID 753 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Product | 1709-72-4 | HCID 9815585 | — |
Reaction Steps
4.6 g of glycerine was dissolved in 50 g of ethyl acetate, to which several drops of triethylamine was added while agitating. Thereafter, a 1,4-dioxane solution of 10 g of acrylic chloride was dropped into the solution, followed by agitating at room temperature for further 2 hours and further agitating for 1 hour after raising the temperature up to 50° C. The reaction solution was discharged and admixed with water, followed by shaking, removing water-soluble components from the system and distilling off the 1,4-dioxane to obtain glycerol-1,3-diacrylate. 10 g (0.05 mole) of the glycerol-1,3-diacrylate, 20.2 g (0.03 mole) of a partially esterified product of styrene/maleic anhydride copolymer ("Styrite CM-2L", molecular weight≈5000, product of Sankyo Kasei Co., Ltd.), 20 mg of hydroquinone were dissolved in 85 g of 1,4-dioxane and agitated at 90° C for 4 hours, followed by dropping the reaction solution into 3 liters of water and drying the resulting precipitate in vacuo, thereby obtaining a carboxylic acid semi-ester polymer (polyfunctional resin).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04537855 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-2cdfa0499c0740d5b7deba37688f5acb |
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| Source note | uspto-grants-1985_08 |
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