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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4348Generated: October 24, 2026

4-(Bromoacetyl)pyridine hydrobromide → 1,1-Difluoro-1-phenyl-[4-(4-pyridyl)-2-thiazolyl]methane

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Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Bromoacetyl)pyridine hydrobromideHCID 2776239—
Reactant2,2-Difluoro-2-phenylethanethioamideHCID 14096960—
SolventEthanolHCID 702—
Product1,1-Difluoro-1-phenyl-[4-(4-pyridyl)-2-thiazolyl]methaneHCID 1409696148%

Reaction Steps

To a solution of 2,2-difluoro-2-phenylthioacetamide (1.57 g, 0.0092 mol) in 95% ethanol (20 mL) was added α-bromo-4-acetylpyridine hydrobromide (3.20 g, 0.012 mol) and the mixture warmed on a steam bath for thirty minutes. The product was isolated in the usual way and recrystallized from ethyl acetate/hexane to afford 1,1-difluoro-1-phenyl-[4-(4-pyridyl)-2-thiazolyl]methane (1.27 g, 48%). mp. 54.5°-55.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04725606
Source datasetuspto-grants-1988_02
ORD IDord-ee8a5d8d7a7843959078967aa73d7741
Source noteuspto-grants-1988_02