HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Butanol → Butyl Acrylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | HCID 20255446 | HCID 20255446 | — |
| Catalyst | Hydroquinone | HCID 785 | — |
| Catalyst | Potassium Cyanide | HCID 9032 | — |
| Product | Butyl Acrylate | HCID 8846 | 96.7% |
Reaction Steps
500 g of ethylacrylate (5 mole), 92.5 g of n-butanol (1.25 mole) and 0.148 g of hydroquinone (250 ppm) are added to a 1 liter round-bottomed flask. By conducting air through by way of a 1 m vigreux column, the azeotrope is dehydrated. After cooling of the contents of the flask to 60° to 70° C., 6 g of potassium cyanide (1%) are added, and the ethylacrylate/ethanol-azeotrope is distilled-off at 77° C. at the head of the column. After 4 to 5 hours, the trans-esterification is completed. After cooling down of the flask, the potassium cyanide is filtered off and the filter residue is washed out with a little ethyl acrylate. The filtrate is processed by fractional distillation. 155 g of n-butyl acrylate = 97% are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04117238 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-919396cb483844da9272a4fc4e26a910 |
| Source note | uspto-grants-1978_09 |