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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-Bromopyridine-4-carboxaldehyde | HCID 2762997 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-Bromo-4-(dimethoxymethyl)pyridine | HCID 20715145 | 96.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946260B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-94b7ec8671794e2c90f43b79de571854 |
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| Source note | uspto-grants-2015_02 |
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