Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Bromoheptane | HCID 12369 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Bromo-4-hydroxybenzoic acid | HCID 84368 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19884404 | HCID 19884404 | — |
Reaction Steps
25.8 g (0.119 mol) of the 3-bromo-4-hydroxybenzoic acid prepared in Step I was dissolved in 615 ml ethanol and 42.6 g (0.238 mol) of heptyl bromide was added to the solution. Aqueous potassium hydroxide (13.5 g of potassium hydroxide in 62 ml of water) was added with heating and the above solution was refluxed for ten hours. 125 ml of 10% aqueous potassium hydroxide was added and the solution was refluxed for two more hours. The reaction solution was allowed to stand to cool to room temperature, and excess 5 N hydrochloric acid solution was added commencing crystallization. The crystals were fractionated through filtration by suction, washed with water, dried and recrystallized with ethanol to yield 32.2 of purified 3-bromo-4-n-heptyloxybenzoic acid. The yield was calculated to be 85.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04341652 |
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| Source dataset | uspto-grants-1982_07 |
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| ORD ID | ord-cc99caa259684903b744da8c9c067603 |
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| Source note | uspto-grants-1982_07 |
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