HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichlorobenzene → HCID 19910814, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichlorobenzene | HCID 7239 | — |
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | 2,5-Bis(4-nitrophenyl)-3,4-diphenylcyclopenta-2,4-dien-1-one | HCID 53701108 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 19910814 | HCID 19910814 | — |
Reaction Conditions
| Temperature | 180 °C |
|---|
Reaction Steps
1,4-bis(4-nitrophenyl)-2,3,5-triphenylbenzene was prepared according to the procedure described in L. F., "Organic Experiments", 2nd Ed., 297 (1968). 19.3 grams (0.189 moles) of phenylacetylene, 20.0 grams (0.0362 moles) of 2,5-bis(4-nitrophenyl)-3,4-diphenylcyclopentadienone, a compound of formula (II) where Ar1 and Ar2 are phenyl, and 130 mL of o-dichlorobenzene were stirred at 180° C. for 2 hours. The reaction mixture was cooled, poured into 500 mL of hexane and filtered. The reaction yielded 22.9 grams of 1,4-bis(4-nitrophenyl)-2,3,5-triphenylbenzene, a 66% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05087691 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-8208ce6f177d41b58d05bfe598099cf6 |
| Source note | uspto-grants-1992_02 |