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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648075Generated: October 26, 2026

Methyl 9-bromononanoate → (E)-9-[3-(6-Hydroxy-1-hexynyl)-2-(3-methoxy-3-oxo-1-propenyl)phenoxy]nonanoic Acid Methyl Ester

https://huagongshe.com/reaction/1648075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 9-bromononanoateHCID 554142—
Reactant(E)-3-[2-Hydroxy-6-(6-hydroxy-1-hexynyl)phenyl]-2-propenoic Acid Methyl EsterHCID 67780365—
Product(E)-9-[3-(6-Hydroxy-1-hexynyl)-2-(3-methoxy-3-oxo-1-propenyl)phenoxy]nonanoic Acid Methyl EsterHCID 6778005371%

Reaction Steps

Using the procedure of example 122, (E)-3-[2-hydroxy-6-(6-hydroxy-1-hexynyl)phenyl]-2-propenoic acid methyl ester (example 176) was alkylated with methyl 9-bromononanoate giving the title compound, in 71% yield, as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05434186
Source datasetuspto-grants-1995_07
ORD IDord-530d227ad6bb4b8cb1504ee6a22d5e1d
Source noteuspto-grants-1995_07