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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097477Generated: October 30, 2026

Hydrochloric Acid → 1-Bromo-3-cyclopropylmethoxy-4-difluoromethoxy-2-iodobenzene

https://huagongshe.com/reaction/2097477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChlorodifluoromethaneHCID 6372—
ReactantSodium HydroxideHCID 14798—
Reactant4-Bromo-2-cyclopropylmethoxy-3-iodophenolHCID 57571709—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
Product1-Bromo-3-cyclopropylmethoxy-4-difluoromethoxy-2-iodobenzeneHCID 6660282392.1%

Reaction Steps

To 20 ml of toluene solution containing 1.84 g (5.0 mmol) of 4-bromo-2-cyclopropylmethoxy-3-iodophenol obtained in Reference example 12-(d) were added 0.8 g (2.5 mmol) of tetrabutylammonium bromide and 10 ml of 35% aqueous solution of sodium hydroxide, and then, 5.0 g (62 mmol) of chlorodifluoromethane was blown thereinto at 80° C. over 30 minutes. After completion of the reaction, 2N hydrochloric acid was added to the reaction mixture to adjust a pH thereof to 5. The organic layer after separation was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The obtained residue was applied to silica gel column chromatography (Eluent; hexane:ethyl acetate=9:1 (V/V)), and the fractions containing the desired compound were concentrated under reduced pressure to obtain 1.93 g of the title compound as a colorless oil. (Yield: 92%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450319B2
Source datasetuspto-grants-2013_05
ORD IDord-6301fb8ea07044d18c6d3144ca58b20b
Source noteuspto-grants-2013_05