Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Methyl Methacrylate | HCID 6658 | — |
| Reactant | 4-Methoxyphenol | HCID 9015 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Methyl methacrylate methanol | HCID 19593510 | — |
| Product | Butyl Methacrylate | HCID 7354 | — |
Reaction Steps
400 g of methyl methacrylate (4 mole), 148 g of n-butanol (2 mole), 2.74 g of potassium cyanide (0.5%) and 0.137 g of hydroquinone monomethyl ether (250 ppm) are added to a 1 liter round-bottomed flask. The batch is heated to approximately 75° C. by conducting air through, and at a temperature of 65° C. at the head of the column, the methyl methacrylate/methanol-azeotrope is distilled-off by way of a 1 m vigreux column. After 4 hours, the trans-esterification is finished. After cooling 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. There results a residue of n-butyl methacrylate of 280 g = 98.5%. The n-butyl methacrylate thus obtained can be used without any further processing.
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-68e7d3bf6a0a46e1ac17b44044879071 |
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| Source note | uspto-grants-1978_09 |
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