HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-(p-Cyclohexyloxybenzoyl)propionic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | Benzene, (cyclohexyloxy)- | HCID 137492 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 3-(p-Cyclohexyloxybenzoyl)propionic acid | HCID 20352630 | — |
Reaction Steps
A solution of succinic anhydride (20 g.) and phenoxycyclohexane (35.1 g.) in 1,2-dichloroethane (250 ml.) was stirred at 0° C and treated with powdered anhydrous aluminium chloride (58.2 g.) and stirring was continued for 5 hours at 0°-5° C. It was then poured carefully with stirring into ice-water (1 liter) containing concentrated hydrochloric acid (100 ml.). The organic layer was separated, washed with water and extracted with a solution of sodium hydroxide (8 g.) in water (250 ml.). The alkaline extract was adjusted to pH 4-6 by the addition of dilute hydrochloric acid to yield the product (6.8 g.), m.p. 190°-192° C after crystallisation from aqueous methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04088762 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-3de6d33631a9455b9b4da2f7548e7a61 |
| Source note | uspto-grants-1978_05 |