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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29500Generated: October 26, 2026

5-Chloro-2-nitrobenzaldehyde → (5-Chloro-2-nitro-phenyl)-(6-chloro-pyridin-3-yl)-methanol

https://huagongshe.com/reaction/29500

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2-nitrobenzaldehydeHCID 81123—
Reactant2-Chloro-5-iodopyridineHCID 4397176—
ReactantHCID 178420663HCID 178420663—
SolventTetrahydrofuranHCID 8028—
Product(5-Chloro-2-nitro-phenyl)-(6-chloro-pyridin-3-yl)-methanolHCID 22327314—

Reaction Conditions

Temperature-45 °C

Reaction Steps

A solution of 1.0 g 2-chloro-5-iodopyridine (4.1 mmol, 1.0 eq.) in 10 mL anhyd. THF was stirred at −40° C. to −50° C. After five minutes, 2.2 mL of 2.1 M iPrMgBr/THF (4.6 mmol, 1.1 eq.) were added drop wise over 1 minute and the reaction mixture is maintained at −40 to −50° C. for 30 minutes. 1.3 g 2-nitro-5-chlorobenzaldehyde (7.0 mmol, 1.7 eq.) was then added and the reaction was maintained at −50° C. After 1 hour, the reaction was allowed to warm to −10° C., and quenched with 50 mL saturated brine after a further fifteen minutes. The crude product was extracted with EtOAc, dried on Na2SO4 and concentrated by rotary evaporation to yield desired product. MS: (M+H)/z=298.9

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420055B2
Source datasetuspto-grants-2008_09
ORD IDord-63a7bf13d186452bada32640db498840
Source noteuspto-grants-2008_09