Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trichlorofluoromethane | HCID 6389 | — |
| Reactant | Dichlorodifluoromethane | HCID 6391 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | AlCl3 CFCl3 | HCID 131717984 | — |
Reaction Steps
500 g (3.75 mol) of AlCl3 (Aldrich-99% pure) was stirred mechanically under N2 in a r.b. flask fitted with a -80° C.. condenser while 1750 mL (~2625 g, 19 mol) of CFCl3 was added over a 1.5-hr period. Reaction is very exothermic in the early stages, so addition of CFCl3 was slow at first in order to keep the temperature below 65° C., then rapid. The resulting suspension was stirred an additional 3 hrs while volatiles (CF2Cl2) were allowed to escape through the warmed condenser. The condenser was then replaced with a simple stillhead, and most of the CCl4 was distilled under reduced pressure [mainly bp 38° C. (200 mm)]. Finally, the last traces of volatiles were removed by warming the residual solid to 30-35° C. at 0.05 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05929293 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-40efb6adcc794e8b895a3920fc408bec |
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| Source note | uspto-grants-1999_07 |
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