Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | 1-Butene | HCID 7844 | — |
| Reactant | Isobutylene | HCID 8255 | — |
| Product | 2,4,4-Trimethyl-1-pentene | HCID 7868 | — |
| Product | Isobutylene | HCID 8255 | — |
Reaction Steps
Into a 300 ml pressure-resistant glass autoclave were charged 10 g of isobutylene, 10 g of 1-butene, 50 g of sulfuric acid and 50 g of water, and the mixture was stirred at 60° C. at a pressure of 8.5 atms for one hour. As a result, isobutylene was hydrated to form tert-butanol with the conversion of 90% and the selectivity to tert-butanol of 92%. At the same time, diisobutylene and the trimer of isobutylene were produced at a yield of 2% and 6%, respectively, and 1-butene was hydrated to form sec-butanol at a yield of 4%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04236034 |
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| Source dataset | uspto-grants-1980_11 |
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| ORD ID | ord-40f12d48f3494f3a8abc6c09cfb540f6 |
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| Source note | uspto-grants-1980_11 |
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