HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636249Generated: October 30, 2026
Hydrochloric Acid → 4-Cyanophenyl cyclopropyl ketone
https://huagongshe.com/reaction/636249
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Bromophenyl cyclopropyl ketone | HCID 81394 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Catalyst | Iron chloride (FeCl3) | HCID 24380 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Cyanophenyl cyclopropyl ketone | HCID 10797264 | — |
Reaction Steps
22.5 g of 4-bromophenylcyclopropylmethanone (100 mmol) and 10.3 g of CuCN (100 mmol) are dissolved in 15 ml of DMF and heated under reflux, with stirring, for 4 hours. The suspension is allowed to cool down to 70° C. and is then poured into a solution consisting of 40 g of iron(III) chloride, 10 ml of conc. HCl and 60 ml of water. The mixture is stirred at 70° C. for 20 minutes. It is then extracted three times with 90 ml of toluene on each occasion. The combined organic phases are washed with 250 ml of 2N hydrochloric acid and with 250 ml of 2N sodium hydroxide solution, and then concentrated. The solid residue is triturated with petroleum ether and filtered off with suction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06191282B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-0aa1663d992d42c096efffb88880d13e |
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| Source note | uspto-grants-2001_02 |
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