HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → HCID 53929976, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 53699764 | HCID 53699764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 53929976 | HCID 53929976 | — |
Reaction Steps
To 38 g of α-[p-(1-cyclooctenyl)-phenoxy]-dodecanoic acid ethyl ester in 150 ml of ethanol are added 150 ml of 2N sodium hydroxide solution and the mixture is stirred for 2 hours at room temperature. The reaction mixture is then evaporated to dryness in vacuo and the residue partitioned between N hydrochloric acid and ether. The organic phases are washed until neutral, dried over sodium sulphate and evaporated to dryness in vacuo. The residue is distilled under a high vacuum at 0.05 mm and 235°-239° C. The distillate is cyrstallised from pentane to yield the α-[p-(1-cyclooctenyl)-phenoxy]-dodecanoic acid of the formula ##STR14## which melts at 45°-48° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04115416 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-04ee762560ef4d068e8725b7a2b6802e |
| Source note | uspto-grants-1978_09 |