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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846559Generated: October 31, 2026

Hydrochloric Acid → (+)-2-Methyloctanoic acid 4-(2-methyloctanoyl) biphenyl

https://huagongshe.com/reaction/846559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2-Methyl octanoic acid chlorideHCID 12812232—
Reactant(+)-2-Methyloctanoic acid biphenylHCID 67826054—
SolventNitrobenzeneHCID 7416—
Product(+)-2-Methyloctanoic acid 4-(2-methyloctanoyl) biphenylHCID 6791376049%

Reaction Conditions

Temperature0 °C

Reaction Steps

Next, 2.02 g (11.4 mmol) of the above (+)-2-methyloctanoic acid chloride and 3 ml of nitrobenzene were charged into a flask, and cooled to 0° C., to which was added 3.06 g (22.9 mmol) of anhydrous aluminum chloride with stirring and then the resulting mixture was stirred at room temperature for 30 minutes. This mixture was added with a solution of 2.89 g (7 mmol) of (+)-2-methyloctanoic acid biphenyl dissolved in 3 ml of nitrobenzene, which was reacted at room temperature for 140 hours with stirring. After the completion of the reaction, 2N hydrochloric acid and ice were added, and the extraction with chloroform was carried out, and the extract was washed with water, dried on anhydrous magnesium sulfate, distilled to remove the solvent, and purified by a column chromatography of silica gel to obtain 1.55 g (yield 49%) of an oily (+)-2-methyloctanoic acid-4-(2-methyloctanoyl) biphenyl.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05137653
Source datasetuspto-grants-1992_08
ORD IDord-e4d8a46715dd4bb5804583d7414ffe70
Source noteuspto-grants-1992_08