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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534142Generated: November 2, 2026

1,2-Dichlorobenzene → HCID 19910814, compound

https://huagongshe.com/reaction/1534142

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichlorobenzeneHCID 7239—
ReactantPhenylacetyleneHCID 10821—
Reactant2,5-Bis(4-nitrophenyl)-3,4-diphenylcyclopenta-2,4-dien-1-oneHCID 53701108—
SolventHexaneHCID 8058—
ProductHCID 19910814HCID 19910814—

Reaction Conditions

Temperature180 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05087691
Source datasetuspto-grants-1992_02
ORD IDord-8208ce6f177d41b58d05bfe598099cf6
Source noteuspto-grants-1992_02