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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710608Generated: October 26, 2026

2-Bromo-4-nitrophenol → 2-Bromo-1-(difluoromethoxy)-4-nitrobenzene

https://huagongshe.com/reaction/1710608

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-4-nitrophenolHCID 22109—
Reactant2-Chloro-2,2-difluoroacetophenoneHCID 238296—
Product2-Bromo-1-(difluoromethoxy)-4-nitrobenzeneHCID 13314704—

Reaction Steps

The compound was prepared starting from commercially available 2-bromo-4-nitrophenol, which was reacted with 2-chloro-2,2-difluoroacetophenone (J. Hu et al., J. Org. Chem., 2006, 71, 9845) to yield 2-bromo-1-difluoromethoxy-4-nitro-benzene. Subsequent Buchwald-Hartwig coupling of 2-bromo-1-difluoromethoxy-4-nitro-benzene with tert.butyloxycarbonyl-piperazine by analogy to preparation example 3.1, reduction of the nitro group to the corresponding aniline by analogy to preparation example 3.2, subsequent coupling with commercially available 2-difluoromethoxybenzene-sulfonylchloride by analogy to preparation example 1.4, and final deprotection under acidic conditions by analogy to example 1 yielded the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790727B2
Source datasetuspto-grants-2010_09
ORD IDord-300dfa31e44440ff94595fdfd52190d2
Source noteuspto-grants-2010_09