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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948272Generated: November 1, 2026

4-Chloro-2-fluorobenzyl bromide → HCID 58966916, compound

https://huagongshe.com/reaction/1948272

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-2-fluorobenzyl bromideHCID 2736551—
ReactantHCID 69345451HCID 69345451—
ProductHCID 58966916HCID 589669161%

Reaction Steps

According to Scheme 31 Step 4: The title compound was prepared from 2-methoxy-4-(methoxymethyl)-5-(4-methoxyphenyl)pyridine (1 eq, 0.66 mmol, 0.17 g) and 1-(bromomethyl)-4-chloro-2-fluorobenzene (1.5 eq, 0.98 mmol, 0.22 g) according to the procedure described for Example 6 Step 2. Reaction conditions: 12 hours at 80° C. The crude product was purified by silica gel chromatography (AIT Flashsmart prepacked column 25 g SiO2) using CH2Cl2/MeOH 98/2 as the eluent to afford 1-(4-chloro-2-fluorobenzyl)-4-(methoxymethyl)-5-(4-methoxyphenyl)pyridin-2(1H)-one (5 μmol, 2 mg, 1%) as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399493B2
Source datasetuspto-grants-2013_03
ORD IDord-0952f781e32444c889331ac7b64fc4e9
Source noteuspto-grants-2013_03