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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246661Generated: October 30, 2026

Chlorodifluoromethane → 1,3-Dibromo-5-(difluoromethoxy)benzene

https://huagongshe.com/reaction/1246661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorodifluoromethaneHCID 6372—
Reactant3,5-DibromophenolHCID 12280—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventPotassium HydroxideHCID 14797—
Product1,3-Dibromo-5-(difluoromethoxy)benzeneHCID 2190464080%

Reaction Steps

To a tared, sealed 350 mL round-bottomed pressure flask containing a solution of 3,5-dibromophenol (10.0 g, 39.7 mmol; see Example 27(ii) above) in 2-propanol (100 mL) and 30% KOH (80 mL) at −78° C. was added chlorodifluoromethane via bubbling for 15 min through the septum. The septum was replaced with a Teflon stopper and the flask was then sealed and allowed to warm to room temperature where the flask was weighed and determined to contain 12.0 g (138 mmol) of chlorodifluoromethane. The solution was refluxed overnight in an oil bath set at 80° C. The flask was cooled to room temperature, the pressure cautiously released and the contents diluted with H2O (200 mL). The aqueous layer was extracted with CHCl3 (2×150 mL), then the combined organics were dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by Kugelrohr distillation at 80° C. at 0.2 mm Hg to afford the sub-title compound (9.6 g, 80%) as clear liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129233B2
Source datasetuspto-grants-2006_10
ORD IDord-6f4782c52bf34aa78a447b08f1c2c679
Source noteuspto-grants-2006_10