Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Methacrylate | HCID 6658 | — |
| Reactant | Stearyl Alcohol | HCID 8221 | — |
| Reactant | 4-Methoxyphenol | HCID 9015 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Product | Stearyl methacrylate | HCID 122600 | — |
Reaction Steps
300 g of methyl methacrylate (3 mole), 135 g of stearyl alcohol (0.5 mole), 4.35 g of KCN (1%) and 0.108 g of hydroquinone methyl ether (250 ppm) are added to a 1 liter round-bottomed flask. The mixture is heated to about 75° C. by conducting air through it and the methyl methacrylate/methanol-azeotrope is removed at a temperature of 65° C. at the head of the column by way of a 1 m vigreux column. The trans-esterification is completed after 3.5 hours. After cooling down of the flask, the sump is filtered to remove the potassium cyanide, and the filter residue is washed with a little methyl methacrylate. The filtrate is concentrated at 40° C. under a water jet vacuum. A white, crystalline residue of stearyl methacrylate of 162 g = 96% will result.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04117238 |
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| Source dataset | uspto-grants-1978_09 |
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| ORD ID | ord-45e06bf162dd41209c860029ac67eea3 |
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| Source note | uspto-grants-1978_09 |
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