HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-[p-(1-Cyclooctenyl)-phenoxy]-heptanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | alpha-[p-(1-Cyclooctenyl)-phenoxy]-heptanoic acid ethyl ester | HCID 54549182 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[p-(1-Cyclooctenyl)-phenoxy]-heptanoic acid | HCID 54272360 | — |
Reaction Steps
To 33 g of α-[p-(1-cyclooctenyl)-phenoxy]-heptanoic acid ethyl ester in 120 ml of ethanol are added 120 ml of 2N sodium hydroxide solutuion and the mixture is stirred for 11/2 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 phase is washed until neutral, dried over sodium sulphate and evaporated to dryness in vacuo. The residue is crystallised from pentane to yield the 2-[p-(1-cyclooctenyl)-phenoxy]-heptanoic acid of the formula ##STR8## (m.p. 57°-60° C; b.p. 0.04 185°-188° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04115416 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-59a83047f9844651896f37969df9d72b |
| Source note | uspto-grants-1978_09 |