Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromopropane | HCID 7840 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-(2-Hydroxybenzoyl)propionic acid | HCID 3016086 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 20352632 | HCID 20352632 | — |
Reaction Steps
3-(o-Hydroxybenzoyl)propionic acid (14.6 g.) was dissolved in n-butanol (300 ml.) containing 85% potassium hydroxide (10 g.) and the resultant solution was treated with 1-bromopropane (24.6 g.) and the mixture heated at reflux temperature for 4 hours. It was then cooled, filtered to remove potassium bromide and the filtrate washed with cold water. The butanol was evaporated at reduced pressure and the residual oil distilled at 0.3 mm when the fraction b.p. 160°-180° C was collected (16.4 g.). This was dissolved in methanol (50 ml.), treated with 20% sodium hydroxide solution (20 ml.) and heated on the steambath for 30 minutes. The methanol was boiled off and the residue diluted with water (250 ml.) and acidified with hydrochloric acid. The precipitated acid was collected and crystallised from 50% methanol. It had m.p. 77°-79° C (Yield 13.3 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04088762 |
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| Source dataset | uspto-grants-1978_05 |
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| ORD ID | ord-aa9638a7b6f74518b60d146a855110bb |
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| Source note | uspto-grants-1978_05 |
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