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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948271Generated: October 30, 2026

N-bromobutanimide → 4-(Bromomethyl)-2-methoxy-5-(4-methoxyphenyl)pyridine

https://huagongshe.com/reaction/1948271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 69344963HCID 69344963—
SolventCarbon TetrachlorideHCID 5943—
Product4-(Bromomethyl)-2-methoxy-5-(4-methoxyphenyl)pyridineHCID 69345327103.2%

Reaction Steps

According to Scheme 31 Step 2: To a solution of 2-methoxy-5-(4-methoxyphenyl)-4-methylpyridine (2.20 mmol, 0.50 g, Example 48 Step 1) in CCl4 (10 mL) was added NBS (2 eq, 4.40 mmol, 0.78 g). The reaction was then heated to reflux and subjected to UV light for 48 hours. The reaction was allowed to cool, filtered and concentrated under reduced pressure to afford crude 4-(bromomethyl)-2-methoxy-5-(4-methoxyphenyl)pyridine (0.70 g) as a yellow oil which was used without any purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399493B2
Source datasetuspto-grants-2013_03
ORD IDord-c7bd0ffc02974cc59284b6965293961f
Source noteuspto-grants-2013_03