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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073474Generated: November 1, 2026

Hydrochloric Acid → (+)-4-(2-Methyloctanoyl) biphenyl 2-methyloctanoate

https://huagongshe.com/reaction/1073474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2-Methyl octanoic acid chlorideHCID 12812232—
Reactant(+)-Biphenyl 2-methyloctanoate biphenylHCID 131716695—
SolventNitrobenzeneHCID 7416—
Product(+)-4-(2-Methyloctanoyl) biphenyl 2-methyloctanoateHCID 13171669449%

Reaction Steps

Next, 2.02 g (11.4 mmol) of the above (+)-2-methyl octanoyl chloride and 3 ml of nitrobenzene were cooled to 0° C. in a flask and added with 3.06 g (22.9 mmol) of anhydrous aluminum chloride with stirring, which were stirred at room temperature for 30 minutes. Thereafter, 2.89 g (7 mmol) of (+)-biphenyl-2-methyloctanoate biphenyl dissolved in 3 ml of nitrobenzene was added thereto, which was reacted by stirring at room temperature for 140 hours. After the completion of the reaction, 2 normal hydrochloric acid and ice were added and extracted with chloroform. The extract was washed with water, dried on anhydrous magnesium sulfate and distilled to remove the solvent. The residue was purified through a column chromatography of silica gel to obtain 1.55 g (yield: 49%) of an oily (+)-4-(2-methyloctanoyl) biphenyl-2-methyloctanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04970023
Source datasetuspto-grants-1990_11
ORD IDord-ab71cc87a6e14ab1b29f7fed5de0cda3
Source noteuspto-grants-1990_11