Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | M-Xylene | HCID 7929 | — |
| Reactant | Propylene | HCID 8252 | — |
| Catalyst | Hastelloy C | HCID 11332432 | — |
| Product | 5-Isopropyl-m-xylene | HCID 20833 | — |
Reaction Steps
A reaction was carried out using a Hastelloy C autoclave having an inside volume of 6,000 mL and equipped with an electromagnetic stirrer, a baffle plate, a gas blowing port and a liquid feed port in the same manner as that in Example 1. For the reaction, 2,003 g (18.9 moles) of metaxylene, 943 g (47.1 moles) of anhydrous HF and 715 g (17.0 moles) of propylene were used. After the reaction was terminated, the reaction mixture was fed at a rate of 300 mL per hour together with 600 g per hour of benzene to a distillation column (column internal pressure: 0.38 MPa, 122° C.) in which benzene was recirculated. A benzene solution of 3,5-dimethylcumene was separated and collected from the bottom of the column, while discharging BF3 from the top and HF from a discharge port below the condenser. The benzene solution of 3,5-dimethylcumene obtained from the bottom of the column was condensed using an evaporator and then distilled (column internal pressure: 0.0133 MPa, stage number: 12, a reflux ratio: 10) to obtain 1,925 g of desired 3,5-dimethylcumene (distillation temperature: 129° C.). The purity was 99.2% and isolation yield was 76%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07518025B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-a67c9e9ddeb94e8fb0fd2f784cfbbf28 |
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| Source note | uspto-grants-2009_04 |
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