HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-(4-Bromo-2-fluorophenyl)cyclopropane-1-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-(4-Bromo-2-fluorophenyl)cyclopropane-1-carbonitrile | HCID 58762329 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(4-Bromo-2-fluorophenyl)cyclopropane-1-carboxylic acid | HCID 66662682 | — |
Reaction Steps
A solution of the compound (24.6 g, 102 mmol) obtained in Example 14-2) and potassium hydroxide (46 g, 820 mmol) in ethanol (200 ml) and water (40 ml) was heated to reflux for 7 h. The reaction mixture was cooled to room temperature, and then 5 N hydrochloric acid was added until the reaction mixture was rendered acidic. The deposited solid was collected by filtration, washed with water, and then dried to obtain the title compound (28.7 g, quant.) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08927536B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-b9a9ff72194b4edead0db89d64755508 |
| Source note | uspto-grants-2015_01 |