HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016551Generated: October 25, 2026
Water → 1-oxo-2,3-dihydro-1H-indene-5-carbonitrile
https://huagongshe.com/reaction/1016551
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 5-Bromo-1-indanone | HCID 520695 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Catalyst | Ferrous Chloride | HCID 24458 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-oxo-2,3-dihydro-1H-indene-5-carbonitrile | HCID 312896 | — |
Reaction Steps
9.5 g of 5-bromo-1-indanone and 4.93 g of CuCN are suspended in 10 ml of dimethylformamide and boiled under reflux for 4 hours. A solution of 18 g of iron(II) chloride in 5 ml of concentrated hydrochloric acid with 30 ml of water are added dropwise to the cooled, dark-brown viscous suspension while stirring, and the mixture is then stirred at 70° C. for 30 minutes. The reaction mixture is extracted by shaking three times with 50 ml of toluene, and the combined organic phases are extracted by shaking with 50 ml of 2N hydrochloric acid and 50 ml of 2N sodium hydroxide solution and then washed with water until neutral. The toluene extract is dried over magnesium sulfate and concentrated in vacuo, and the residue is recrystallized from n-heptane. 1-oxoindane-5-carbonitrile is obtained with a melting point of 123-125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06476059B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-20e691d55e2f465dafad5c7d449d818f |
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| Source note | uspto-grants-2002_11 |
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