Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenyl hexanoate | HCID 522678 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | HCID 12642573 | HCID 12642573 | — |
Reaction Steps
24 g (0.18 mole) of powdered aluminium trichloride were carefully added to 31 g (0.16 mole) of phenyl hexanoate and the mixture was slowly heated with occasional stirring to 120° C and was held there for 11/2 hours. The residue was ground into a powder and was poured into iced dilute hydrochloric acid with stirring. The mixture was extracted with ether and the ether extracts were washed with dilute sodium hydroxide solution, then with water, dried over magnesium sulfate and evaporated to dryness to obtain 14.2 of (1-(2'-hydroxyphenyl)-hexan-1one as a pale yellow oil. IR spectrum showed o-hydroxyphenylcarbonyl at 1650cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04024276 |
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| Source dataset | uspto-grants-1977_05 |
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| ORD ID | ord-dc6d9248f6c84421a7f945dc116524d7 |
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| Source note | uspto-grants-1977_05 |
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