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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1080730Generated: October 31, 2026

Bromine → HCID 23365458, compound

https://huagongshe.com/reaction/1080730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant1-(4'-Methyl[1,1'-biphenyl]-2-yl)ethanoneHCID 9837211—
Reactantbromine AcOHHCID 87433071—
SolventAcetic AcidHCID 176—
SolventHexaneHCID 8058—
ProductHCID 23365458HCID 23365458943.7%

Reaction Conditions

Temperature30 °C

Reaction Steps

A solution of 2.06 g (9.79 mmol) of 4'-methyl-2-acetyl-1,1'-biphenyl (Example 4, Step A) in 10 mL of glacial acetic acid was treated dropwise with a solution of bromine (1.722 g, 1.07 mmol) dissolved in 3.0 mL of glacial acetic acid. After initiating the reaction with the first few drops of the bromine/acetic acid reagent by heating the reaction mixture at 30°C., the remainder of the bromine solution was added dropwise at 25°-30° C. The reaction mixture was stirred at room temperature until the consumption of bromine was complete (approximately 2 hrs). The reaction mixture was diluted with 150 mL of hexane then washed with water (3×50 mL). The organic layer was removed, dried over magnesium sulfate, filtered and evaporated under vacuum to give 2.92 g of an oil that was used in the next step without purification. 1H NMR (crude product) (200 MHz, CDCl3): 2.38 (s, 3H), 3.66 (s, 2H), 7.21 (s, 4H), 7.3-7.6 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05583130
Source datasetuspto-grants-1996_12
ORD IDord-d9914078a74143568aede0be420d3ac6
Source noteuspto-grants-1996_12