HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 2,3-Diphenyl-1,3-butadiene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 1,1'-(1,4-Dibromobut-2-ene-2,3-diyl)dibenzene | HCID 54034006 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2,3-Diphenyl-1,3-butadiene | HCID 4129133 | — |
Reaction Steps
The process of this invention for synthesis of 2,3-diphenyl-1,3-butadiene is comprised of a four step procedure wherein the starting compound acetophenone is dimerized under an ultra violet reaction process to yield acetophenone pinacol which is subsequently converted to 2,3-diphenyl-2-butene in the step 2 procedure. The 2,3-diphenyl-2-butene is then reacted with N-bromosuccinimide (NBS) in an ultra violet reactor in a CCl4 reaction solvent to form 1,4-dibromo-2,3-diphenyl-2-butene in the step 3 procedure. The 1,4-dibromo-2,3-diphenyl-2-butene is reacted with NaI in a hot acetone solution to yield 2,3-diphenyl-1,3-butadiene in the step 4 procedure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04665257 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-5b3df1e38e1a4f6981f211a9861351a5 |
| Source note | uspto-grants-1987_05 |