Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 70632612 | HCID 70632612 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 70632583 | HCID 70632583 | — |
Reaction Steps
A solution of 5 g of sodium nitrite in 20 ml of water is slowly added dropwise at 0° C, whilst stirring, to a solution of 11 g of crude 3-amino-4-cycloheptyl-acetophenone in 70 ml of concentrated hydrochloric acid. After completion of the addition the mixture is stirred for a further 30 minutes at 0° C. The reaction solution is then added dropwise at 0° to 5° C, whilst stirring, to a solution of 7 g of freshly prepared copper-(I) chloride in 30 ml of concentrated hydrochloric acid. After completion of the addition, the mixture is stirred for a further hour at room temperature and a further hour at 40° to 50° C. The reaction mixture is now extracted three times with 200 ml of ether at a time. The organic phases are successively washed with water, 2 N sodium hydroxide solution and again with water, dried over sodium sulphate and evaporated in vacuo. Distillation of the evaporation residue in a high vacuum yields crude 3-chloro-4-cycloheptyl-acetophenone in the fraction boiling at about 130° C/0.05 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04004026 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-78e57c34b0594ac9a8f3073b23113635 |
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| Source note | uspto-grants-1977_01 |
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