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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511720Generated: October 31, 2026

Triethylamine → 1-Bromo-4-{difluoro[4-(4,4,4-trifluorobutoxy)phenoxy]methyl}benzene

https://huagongshe.com/reaction/511720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBromineHCID 24408—
ReactantN,N-Diethylethanamine trihydrofluorideHCID 175505—
Reactant4-(4,4,4-Trifluorobutoxy)phenolHCID 67454964—
Reactant2-(4-bromophenyl)-5,6-dihydro-4H-1,3-dithiin-1-ium trifluoromethanesulfonateHCID 86676556—
SolventDichloromethaneHCID 6344—
Product1-Bromo-4-{difluoro[4-(4,4,4-trifluorobutoxy)phenoxy]methyl}benzeneHCID 8667655760.2%

Reaction Conditions

Temperature-55 °C

Reaction Steps

69.3 g (164 mmol) of 2-(4-bromophenyl)-5,6-dihydro-4H-1,3-dithiin-1-ium trifluoromethanesulfonate, are solubilised in 750 mL of dichloromethane. The solution is cooled down to −55° C. 53.94 g (245 mmol) of 4-(4,4,4-trifluorobutoxy)phenol and 36.5 ml (262 mmol) of triethylamine dissolved in 300 ml of dichloromethane is added to the previous solution. The solution was cooled down to −70° C. and stirred for 45 minutes. 120 ml (736 mmol) of triethylamine trihydrofluoride are added to the mixture. A solution of 8.43 ml (164 mmol) of bromine in 60 ml of dichloromethane is added at this temperature. The reaction is stirred for one hour. The reaction is quenched by addition of NaHCO3. The organic phase is washed repeatedly with water, dried over sodium sulfate, filtrated and concentrated under reduced pressure. Chromatography of the residue on 400 g silica gel using toluene: ethyl acetate 95:5 as eluent yields 42 g of 1-bromo-4-{difluoro[4-(4,4,4-trifluorobutoxy)phenoxy]methyl}benzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09097938B2
Source datasetuspto-grants-2015_08
ORD IDord-83684ea9a74e4a04be52b400ea666508
Source noteuspto-grants-2015_08