HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl iodide → 1,2,3,4-Tetrahydro-1,1,6-trimethylnaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | 1-Iodohexane | HCID 12527 | — |
| Reactant | 1-Iodododecane | HCID 20282 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Reactant | Diiodoethane | HCID 68980 | — |
| Reactant | Propane, 2,2-diiodo- | HCID 11483316 | — |
| Reactant | HCID 12554946 | HCID 12554946 | — |
| Reactant | 2,3-Dibromo-1,4-dimethylbenzene | HCID 22638483 | — |
| Product | 1,2,3,4-Tetrahydro-1,1,6-trimethylnaphthalene | HCID 68057 | — |
Reaction Steps
A series of ionene polymers were prepared according to the procedure of Example 1 except that equivalent amounts of iodo-propane, iodo-hexane, iodo-dodecane, iodo-butane or a mixture of dibromobutene and diiodopropane or diiodoethane were substituted for dibromo-p-xylene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04414080 |
| Source dataset | uspto-grants-1983_11 |
| ORD ID | ord-835e17f68a3142999e1e3fc1c979733c |
| Source note | uspto-grants-1983_11 |