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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264359Generated: October 27, 2026

Hydrochloric Acid → 2-acetoxy-4-{(2E)-3,7-dimethylocta-2,6-dienyloxy}benzoic acid

https://huagongshe.com/reaction/264359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetic AnhydrideHCID 7918—
Reactant4-{(2E)-3,7-dimethylocta-2,6-dienyloxy}-2-hydroxybenzoic acidHCID 10424313—
SolventPyridineHCID 1049—
Product2-acetoxy-4-{(2E)-3,7-dimethylocta-2,6-dienyloxy}benzoic acidHCID 6913036248%

Reaction Steps

To 10 ml of a pyridine solution containing 0.82 g (2.82 mmol) of 4-{(2E)-3,7-dimethylocta-2,6-dienyloxy}-2-hydroxybenzoic acid was added 0.72 g (7.1 mmol) of acetic anhydride, followed by stirring at room temperature for 1 hour. The reaction mixture was poured into a 2% hydrochloric acid aqueous solution and extracted with ethyl acetate. The organic layer was washed successively with water and a saturated sodium chloride aqueous solution, dried over sodium sulfate, and concentrated. The resulting crude product was recrystallized from an ethyl ether/hexane mixed solvent to obtain 0.45 g (yield: 48%) of 2-acetoxy-4-{(2E)-3,7-dimethylocta-2,6-dienyloxy}benzoic acid represented by the following structural formula (hereinafter referred to as compound 45) as white crystals. The analytical results are shown below. ##STR66##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646184
Source datasetuspto-grants-1997_07
ORD IDord-169ba451713944ffb01cacfa03df35c5
Source noteuspto-grants-1997_07