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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846555Generated: October 25, 2026

Hydrochloric Acid → 2-Methylbutanoic acid 4-(2-methylbutanoyl) biphenyl

https://huagongshe.com/reaction/846555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantNitrobenzeneHCID 7416—
ReactantButanoyl chloride, 2-methyl-HCID 93697—
ReactantAluminum(III) ChlorideHCID 6451240—
Product2-Methylbutanoic acid 4-(2-methylbutanoyl) biphenylHCID 6791376554%

Reaction Conditions

Temperature0 °C

Reaction Steps

Then, 4.0 g of (+)-2-methylbutanoic acid chloride and 7 ml of nitrobenzene were charged into a flask and cooled to 0° C., to which was added 10.74 g (80 mmol) of aluminum chloride with stirring and further added a solution of 4.97 g (19.6 mmol) of (+) 2-methylbutanoic acid-4-biphenyl in 9 ml of nitrobenzene and then stirred at room temperature for 70 hours. Thereafter, the resulting mixture was added with 2 normal hydrochloric acid and ice and extracted with chloroform. The chloroform layer was washed with water, dried on anhydrous magnesium sulfate, and purified by a column chromatography of silica gel after the distillation off of the solvent to obtain 3.60 g (yield 54%) of oily 2-methylbutanoic acid-4-(2-methylbutanoyl) biphenyl. The NMR analytical values of this purified product were as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05137653
Source datasetuspto-grants-1992_08
ORD IDord-58e799445db4465e80ac4d17f7d08dc9
Source noteuspto-grants-1992_08