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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843970Generated: October 26, 2026

p-Toluenesulfonic acid → 3-Bromo-4-(dimethoxymethyl)pyridine

https://huagongshe.com/reaction/1843970

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantEthyl AcetateHCID 8857—
Reactant3-Bromopyridine-4-carboxaldehydeHCID 2762997—
SolventMethanolHCID 887—
SolventHexaneHCID 8058—
Product3-Bromo-4-(dimethoxymethyl)pyridineHCID 2071514596.3%

Reaction Conditions

Temperature75 °C

Reaction Steps

p-Toluene sulphonic acid (PTSA) (613.5 mg, 3.225 mmol) was added to a stirred solution of 3-bromoisonicotinaldehyde (500 mg, 2.688 mmol) in methanol (20 mL) and the resulting reaction mixture was stirred for 3 hours at 75° C. The reaction was monitored by TLC (10% ethyl acetate in hexane). The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The crude residue was diluted with ice, basified using saturated NaHCO3 solution and extracted using ethyl acetate. The organic layer was washed with water, brine solution, dried over Na2SO4 and concentrated under reduced pressure. Purification by column chromatography on silica gel (10% ethyl acetate in hexane) afforded 600 mg of the product (96.3% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946260B2
Source datasetuspto-grants-2015_02
ORD IDord-94b7ec8671794e2c90f43b79de571854
Source noteuspto-grants-2015_02