HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260291Generated: October 30, 2026
Ethylene Glycol → HCID 21476735, compound
https://huagongshe.com/reaction/260291
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 570263 | HCID 570263 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21476735 | HCID 21476735 | 66.2% |
Reaction Steps
A mixture of 5.0 g of 1-benzoyl-1,2,2a,3,4,5-hexahydrobenz[cd]indol-5-one, 2.7 g of potassium hydroxide, 2 ml of hydrazine hydrate and 20 ml of ethylene glycol was heated at 120° C. for 2 hours and then at 190° C. for 3 hours. After mixture cooling, water was added, and the reaction product was extracted with dichloromethane. After the extract was dried over magnesium sulfate, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: dichloromethane-ethyl acetate=10:1 (v/v)) to yield 1.9 g of 1,2,2a,3,4,5-hexahydrobenz[cd]indole as a colorless crystal having a melting point of 58° to 59° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05527800 |
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| Source dataset | uspto-grants-1996_06 |
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| ORD ID | ord-b0bca5d8be6740e3be04b78bf8efea38 |
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| Source note | uspto-grants-1996_06 |
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