HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 457550Erstellt: 24. Oktober 2026
2-Methyl-2-butene → 4-Iodo-2-methoxypyridine-3-carboxylic acid
https://huagongshe.com/de/reaction/457550
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Methyl-2-butene | HCID 10553 | — |
| Edukt | 4-Iodo-2-methoxynicotinaldehyde | HCID 10038381 | — |
| Edukt | Sodium Chlorite | HCID 23668197 | — |
| Edukt | Monosodium phosphate | HCID 23672064 | — |
| Lösungsmittel | Formic Acid | HCID 284 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | tert-Butanol | HCID 6386 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-Iodo-2-methoxypyridine-3-carboxylic acid | HCID 18439940 | 67% |
Reaktionsschritte
To a solution of 4-iodo-2-methoxy-pyridine-3-carbaldehyde (4.96 g, 18.9 mmol) in 22 mL tert.-butanol was added in this order 2-methyl-2-butene (30 mL of a 2 M solution in THF, 60 mmol), natriumdihydrogen-phosphate (5.7 g, 47.5 mmol), water (15 mL) and sodiumchlorite (3.9 g, 43 mmol). The mixture was stirred at ambient temperature for 1 hour, then poured on dilute aqueous formic acid. The mixture was extracted with ethyl acetate, the organic layer washed with water and brine and concentrated. The residue was dissolved in diisopropylether+dichloromethane (1+1) and extracted 3 times with half-concentrated aqueous NaOH solution. The combined aqueous layers were acidified with conc. HCl and extracted with ethyl acetate. The organic layers were washed with water and brine, then dried over sodium sulfate and concentrated to give 3.462 g of the title compound as a white solid (67%). 1H NMR (500 MHz, CD3OD) δ 7.83 (d, J=5.4 Hz, 1H), 7.43 (d, J=5.4 Hz, 1H), 3.94 (s, 3H);
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07189716B2 |
|---|
| Quelldatensatz | uspto-grants-2007_03 |
|---|
| ORD ID | ord-95f44250f2ae4abf80b18a4681f20a35 |
|---|
| Quellennotiz | uspto-grants-2007_03 |
|---|