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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632144Generated: November 1, 2026

1-Bromooctane → Methyl 3,5-bis(octyloxy)benzoate

https://huagongshe.com/reaction/1632144

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromooctaneHCID 8140—
ReactantMethyl 3,5-DihydroxybenzoateHCID 75076—
ProductMethyl 3,5-bis(octyloxy)benzoateHCID 20443352—

Reaction Steps

200 ml of ethyl alcohol and then 2.3 g of purified sodium are introduced into a 500 ml Erlenmeyer flask. A reflux condenser is fitted to the Erlenmeyer flask and the reaction medium is stirred with a magnetized bar. When the sodium ethylate is formed, 8.4 g of methyl-3,5-dihydroxybenzoate is added, accompanied by stirring. As soon as the medium has become homogeneous, 20.26 g of distilled octyl bromide are added dropwise. Heating under refluxing takes place for 20 hours.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04474679
Source datasetuspto-grants-1984_10
ORD IDord-b16ab4a2e3744e7ba34e93f3c78411af
Source noteuspto-grants-1984_10