HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516660Generated: November 2, 2026
p-Toluenesulfonic acid → HCID 178439035, compound
https://huagongshe.com/reaction/1516660
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Diisopropylaniline | HCID 32484 | — |
| Reactant | 6-Bromopyridine-2-carbaldehyde | HCID 2757009 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178439035 | HCID 178439035 | — |
Reaction Steps
A dry, 500 mL 3-neck round bottom flask is charged with a solution of 2-formyl-6-bromopyridine (72.1 g, 383 mmol) and 2,6-diisopropylaniline (72.5 g, 383 mmol) in 500 mL of anhydrous toluene containing 0.3 nm pore size molecular sieves (6 g) and 80 mg of p-TsOH. The reactor is equipped with a condenser, an over head mechanical stirrer and a thermocouple well. The mixture is heated to 70° C. under N2 for 12 h. After filtration and removal of the volatiles under reduced pressure, a brown oil is isolated. Yield was 109 g, 81.9 percent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08227546B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-e3b6bc9cb5774b8187e0c140a5aa7af0 |
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| Source note | uspto-grants-2012_07 |
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