HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (2-Hydroxy-4-pentadecylphenyl)(phenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 20184921 | HCID 20184921 | — |
| Product | (2-Hydroxy-4-pentadecylphenyl)(phenyl)methanone | HCID 20184914 | — |
Reaction Steps
3-Pentadecylphenyl benzoate (1.366 g) is finely powered, mixed with pulverised anhydrous aluminium chloride (0.616 g) and the intimate miture is heated to 165° during fifteen minutes. After hydrogen chloride evolution has ceased, the cooled mixture is treated with water, concentrated hydrochloric acid added, and the whole thoroughly stirred to decompose the aluminium complex. The product is ethereally extracted and the dried ethereal layer is concentrated to give the crude product (1.348 g) which possesses a greenish ferric chloride reaction. Chromatographic purification and crystallisation from light petroleum (40°-60°) afford 2-hydroxy-4-pentadecylbenzophenone, m.p. 46°-47°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04697038 |
| Source dataset | uspto-grants-1987_09 |
| ORD ID | ord-5ef7882a85354884a13555d04469cddd |
| Source note | uspto-grants-1987_09 |