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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182322Generated: November 3, 2026

Water → 2-Bromo-3',4,4',5-tetrakis(2-methylbutoxy)-1,1'-biphenyl

https://huagongshe.com/reaction/1182322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 17938208HCID 17938208—
SolventEthyl AcetateHCID 8857—
Product2-Bromo-3',4,4',5-tetrakis(2-methylbutoxy)-1,1'-biphenylHCID 1793820992%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

339 g (679.7) mmol of 3,3′,4,4′-tetra(2-methylbutyloxy)biphenyl were dissolved in 800 ml of ethyl acetate. 120.98 g (679.7 mmol) of N-bromosuccinimide were then added in solid form over a period of 15 minutes under protective gas, in the absence of light and with cooling to 0-5° C. The suspension was slowly warmed to room temperature under a blanket of protective gas and was then stirred vigorously at room temperature for 4 hours. 500 ml of ethyl acetate and 300 ml of water were added, the phases were separated and the aqueous phase was extracted twice with 100 ml each time of ethyl acetate. The combined organic phases were washed twice with 50 ml each time of water and dried over MgSO4. The oil obtained was filtered through silica gel with the aid of hexane. Taking off the solvent gave 361.2 g (625.3 mmol, 92%) of 2-bromo-4,5,3′,4′-tetra(2-methylbutyloxy)biphenyl as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07288617B2
Source datasetuspto-grants-2007_10
ORD IDord-2835ee994f5546c2898283b8dad51866
Source noteuspto-grants-2007_10