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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzene | HCID 241 | — |
| Reactant | Phenyl(5a,6,6a,7a-tetrahydro[1]benzoxireno[4,3,2-cd]indol-4(5H)-yl)methanone | HCID 295660 | — |
| Catalyst | zinc(II)iodide | HCID 9883512 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Benzoyl-1,2,2a,5-tetrahydrobenzo[cd]indol-4(3H)-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04110339 |
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| Source dataset | uspto-grants-1978_08 |
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| ORD ID | ord-0d0019a9c7b843e6a8826d6fbc5b2848 |
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| Source note | uspto-grants-1978_08 |
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