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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728551Generated: November 1, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 54288891, compound

https://huagongshe.com/reaction/728551

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantHCID 12582037HCID 12582037—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54288891HCID 54288891—

Reaction Conditions

Temperature0 °C

Reaction Steps

7.2 g (0.034 mol) of 2,3,3a,4,5,6-hexahydro-1H-pyrido[3,2,1-jk]carbazole prepared according to A. S. Baily et al. J. C. S. Perkin I (1980) 97, were dissolved in 300 ml of tetrahydrofuran. The mixture was diluted with 30 ml of water and cooled to 0° C. A solution of 17.0 g (0.075 mol) of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone in 150 ml of tetrahydrofuran was added dropwise in 10 minutes while stirring thoroughly at a reaction temperature between 0° and 5° C. The reaction mixture was stirred for 1 hour and evaporated in vacuum. The residue was extracted with methylene chloride. The methylene chloride solution was washed with 200 ml of 0.5N sodium hydroxide solution and evaporated in vacuum. The residue was chromatographed over 500 g of silicagel using ethyl acetate as an eluent. After evaporating the good fraction, the desired ketone was obtained in a yield of 4.6 g (60%) having a melting-point of 172°-173° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05049563
Source datasetuspto-grants-1991_09
ORD IDord-b6ca8e4e464f45b5ae355b5785b88f33
Source noteuspto-grants-1991_09