Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Phenothiazine | HCID 7108 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acetylacetone | HCID 31261 | — |
| Catalyst | Hafnium | HCID 23986 | — |
| Catalyst | Hafnium chloride (HfCl4) (6CI,8CI); Hafnium chloride; Hafnium tetrachloride; Hafnium(IV) chloride; Hafnium chloride (HfCl4), (T-4)- | HCID 9927068 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Butyl Methacrylate | HCID 7354 | — |
Reaction Steps
An example utilizing an in-situ hafnium catalyst was performed by adding 20.0 g (274 mmol) n-butanol, 135 g (1.35 mole) MMA, 20 mg phenothiazine to a 300 ml round bottom flask equipped with an agitator, thermometer, and Vigreux fractional distillation column. The solution was dehydrated by refluxing the mixture at atmospheric pressure and removing water via a MMA/water azetrope. The mixture was then cooled to 0° C. (ice bath) where 1.63 g (16.1 mmol) triethylamine, 1.0 g (10.0 mmol) 2,4-pentanedione, and 870 mg (2.72 mmol) hafnium tetrachloride were added to the solution. The catalyzed mixture was heated to reflux at 1 atm. pressure while azetropic mixture of MMA and MeOH was removed from the upper part of the fractionating column. The reaction was continued in this manner for approximately 2 hours while the temperature at the top of the column was 65°-67° C. and the temperature in the pot was 97°-112° C. Analysis of the reaction mixture by gas-liquid chromatographic analysis showed greater than 99% conversion of the n-butanol to n-butyl methacrylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05037978 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-36392fea3164472292214cdbab28e555 |
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| Source note | uspto-grants-1991_08 |
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