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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269050Generated: November 1, 2026

Chloroacetaldehyde → HCID 67000913, compound

https://huagongshe.com/reaction/269050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Bromo-5-(4-trifluoromethyl-phenyl)-pyridin-2-ylamineHCID 67000967—
SolventEthanolHCID 702—
ProductHCID 67000913HCID 6700091363%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a mixture of 3-bromo-5-(4-trifluoromethyl-phenyl)-pyridin-2-ylamine (example C.25 step 2) (4.96 g, 16 mmol) and sodium bicarbonate (5.256 g, 63 mmol) in EtOH (20 mL) at 50° C. was dropwise added chloroacetaldehyde (50% in water, 3.66 mL, 31 mmol) within 2 h. Cooled to 23° C. and evaporated all volatiles The residue was purified by silica gel column chromatography with dichloromethane/methanol followed by trituration with heptane and very little ether to give the title compound as a white solid (3.4 g, 63%). MS (ISP) 340.9 [(M+H)+], 343.1 [(M+2+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446113B2
Source datasetuspto-grants-2008_11
ORD IDord-92e41817ecee4c29ad097fa645ffa39b
Source noteuspto-grants-2008_11