HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764133Generated: October 25, 2026
Ethyl 2-bromodecanoate → alpha-[p-(1-Cyclooctenyl)-phenoxy]-decanoic acid ethyl ester
https://huagongshe.com/reaction/1764133
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2-bromodecanoate | HCID 95581 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | p-(1-Cyclooctenyl)-phenol | HCID 53964233 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | alpha-[p-(1-Cyclooctenyl)-phenoxy]-decanoic acid ethyl ester | HCID 54371422 | — |
Reaction Steps
To 2.1 g of sodium in 100 ml of absolute ethanol are added stirring 15 g of p-(1-cyclooctenyl)-phenol. After stirring has continued for a further 30 minutes, 31.5 g of 2-bromo-decanoic acid ethyl ester are slowly added dropwise to this solution and the mixture is maintained at 50° C for 24 hours. After the solvent has been removed in vacuo, the residue is partitioned at 0° C between ether and 2N sodium hydroxide solution. The organic phase is washed until neutral, dried over sodium sulphate and evaporated in vacuo, to thus yield the oily α-[p-(1-cyclooctenyl)-phenoxy]-decanoic acid ethyl ester of the formula ##STR11##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04115416 |
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| Source dataset | uspto-grants-1978_09 |
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| ORD ID | ord-3eab82b40ec3499eb7074e4b4a413374 |
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| Source note | uspto-grants-1978_09 |
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