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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566622Generated: October 25, 2026

Ethyl 10-undecenoate → Ethyl 10-Bromodecanoate

https://huagongshe.com/reaction/566622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 10-undecenoateHCID 12729—
ReactantPhosphorus tribromideHCID 24614—
ReactantSodium borohydrideHCID 4311764—
ReactantDecanoic acid, 10-hydroxy-, ethyl esterHCID 21266885—
ProductEthyl 10-BromodecanoateHCID 560452—

Reaction Steps

The order of functionalization and esterification is not critical. For example, rather than performing an ozonolysis of the starting material, for example, 10-undecylenic acid, as described above, the starting material first may be esterified with ethanol or other alcohol to form an ester, for example, ethyl 10-undecylenate. Next, the ester can undergo functionalization by first ozonating the ester and then reducing the ozonide using, for example, sodium borohydride to form a hydroxylated ester, for example, ethyl 10-hydroxydecanoate. The hydroxylated ester finally is converted to the desired functionalized ester using, for example, PBr3 to form ethyl 10-bromodecanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06175024B1
Source datasetuspto-grants-2001_01
ORD IDord-f01fe87e9ea34abfb07583586c143025
Source noteuspto-grants-2001_01