Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Vinylidene chloride | HCID 6366 | — |
| Reactant | Hexane, 2,5-dichloro-2,5-dimethyl- | HCID 80360 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | HCID 15919150 | HCID 15919150 | — |
Reaction Steps
At 0° C. under agitation, 3.75 g of aluminum chloride is added in portions within 45 minutes to a thoroughly stirred suspension of 54.9 g of 2,5-dichloro-2,5-dimethylhexane in 135 ml of 1,1-dichloroethylene. The reaction mixture is then stirred for another 100 minutes at 0° C. and combined with 10 ml of water and 20 g of anhydrous calcium chloride. The mixture is then filtered and the excess 1,1-dichloroethylene removed under vacuum. Yield: 88.4 g of a viscous oil from which, by solid-matter distillation, 17.5 g of 2,5-dichloro-2,5-dimethylhexane is recovered. The residue is distilled, thus obtaining 34.3 g of 1,1,1,6-tetrachloro-3,3,6-trimethylheptane as a slightly yellow oil, boiling point 79°-80° C. under 0.5 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04816602 |
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| Source dataset | uspto-grants-1989_03 |
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| ORD ID | ord-c383103f8b144606b69d593e242130a2 |
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| Source note | uspto-grants-1989_03 |
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