HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 42142Erstellt: 23. Oktober 2026
Ammonium Chloride → 5-Bromo-2-(4-methanesulfonylbenzyloxy)pyridine
https://huagongshe.com/de/reaction/42142
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 2,5-Dibromopyridine | HCID 69353 | — |
| Edukt | (4-Methanesulfonylphenyl)methanol | HCID 3801026 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 5-Bromo-2-(4-methanesulfonylbenzyloxy)pyridine | HCID 67083256 | 31% |
Reaktionsschritte
A solution of 2,5-dibromopyridine (474 mg, 2.00 mmol) and 4-(methanesulfonyl)benzyl alcohol (372 mg, 2.00 mmol) in tetrahydrofuran (5 mL) was cooled to −15° C. under N2 and potassium tert-butoxide (1.0M in tetrahydrofuran, 2.2 mL, 2.20 mmol) was added dropwise over 10 minutes. The mixture was stirred at 0° C. for 5.5 hours, poured into saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/1) to give the title compound (210 mg, yield 31%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08536176B2 |
|---|
| Quelldatensatz | uspto-grants-2013_09 |
|---|
| ORD ID | ord-c78bc94182cb42c48b59f4800f97a3c8 |
|---|
| Quellennotiz | uspto-grants-2013_09 |
|---|