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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420257Generated: November 3, 2026

Benzene → 1-Benzoyl-1,2,2a,5-tetrahydrobenzo[cd]indol-4(3H)-one

https://huagongshe.com/reaction/2420257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantPhenyl(5a,6,6a,7a-tetrahydro[1]benzoxireno[4,3,2-cd]indol-4(5H)-yl)methanoneHCID 295660—
Catalystzinc(II)iodideHCID 9883512—
SolventEthyl AcetateHCID 8857—
Product1-Benzoyl-1,2,2a,5-tetrahydrobenzo[cd]indol-4(3H)-oneHCID 295664—

Reaction Steps

Twenty grams of 1-benzoyl-4,5-epoxy-1,2,2a,3,4,5-hexahydrobenz[cd]indole were dissolved in 500 ml. of benzene. 7.7 g. of zinc iodide were added and the resulting mixture refluxed under nitrogen for about 1.5 hours. Thin layer chromatrography indicated one major spot slightly slower than the spot corresponding to starting material. The reaction mixture was cooled and then diluted with ethyl acetate. The resulting organic layer was washed with water, and with saturated aqueous sodium chloride and was then dried. Evaporation of the solvent yielded a residue comprising 1-benzoyl-4-keto-1,2,2a,3,4,5-hexahydrobenz[cd]indole formed in the above reaction. The residue was crystallized by trituration with ether containing a small amount of benzene, yielding crystals melting at 146°-149° C. (yield equals 16.9 g.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04110339
Source datasetuspto-grants-1978_08
ORD IDord-0d0019a9c7b843e6a8826d6fbc5b2848
Source noteuspto-grants-1978_08