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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465877Generated: October 25, 2026

1-Bromooctadecane → 3,5-Dioctadecyloxybenzoic acid ethyl ester

https://huagongshe.com/reaction/465877

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromooctadecaneHCID 8218—
ReactantBenzoic acid, 3,5-dihydroxy-, ethyl esterHCID 20098—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
Product3,5-Dioctadecyloxybenzoic acid ethyl esterHCID 53731475—

Reaction Steps

50 m mol of 3,5-dihydroxybenzoic acid ethyl ester, 120 m mol of stearyl bromide, and 110 m mol of sodium were made to react in ethanol, thereby forming 35 m mol of 3,5-dioctadecyloxybenzoic acid ethyl ester. This ester, 25 m mol, was first hydrolyzed into the corresponding acid, which in turn was converted into its acid chloride. The acid chloride was reacted in the same way as in Example 1, whereby 10 m mol of N-(3,5-dioctadecyloxybenzoyl)-N'methylsulfonyl-p-quinonediimine was obtained which is represented by the following formula: ##STR30##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05153680
Source datasetuspto-grants-1992_10
ORD IDord-0708f62d736c4ba789917a02358715dc
Source noteuspto-grants-1992_10