HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7760Erstellt: 24. Oktober 2026
Ethyl Acetate → 5-(1,3-Benzoxazol-2-yl)-2-pyridin-2-yl benzonitrile
https://huagongshe.com/de/reaction/7760
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | 2-(Tributylstannyl)pyridine | HCID 607784 | — |
| Edukt | 4-(1,3-Benzoxazol-2-yl)-2-cyanophenyl trifluoromethanesulfonate | HCID 21990967 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | 1,2-Dimethoxyethane | HCID 8071 | — |
| Lösungsmittel | Sodium chloride; water | HCID 57417360 | — |
| Produkt | 5-(1,3-Benzoxazol-2-yl)-2-pyridin-2-yl benzonitrile | HCID 10236467 | — |
Reaktionsschritte
The degassed solution of 4-(1,3-benzoxazol-2-yl)-2-cyanophenyl trifluoromethanesulfonate (300 mg, 1.2 mmol) in DME (5 mL) was added 2-tri-n-butylstannylpyridine (273 mg, 0.74 mmol), tetrakis(triphenylphosphine)palladium(0) (150 mg, 0.1 mmol). The reaction was stirred at 90° C. overnight and cooled to rt. EtOAc (100 mL) was added, as well as brine (50 mL). The organic layer was washed with brine (2×20 mL), dried (MgSO4), and the crude material was purified on flash column (silica gel, hexanes:EtOAc 3:1) to afford desired 5-(1,3-benzoxazol-2-yl)-2-pyridin-2-yl benzonitrile as pinkish solid. 1H NMR (CD3OD, 300 MHz), δ 8.85 (d 1H), 8.72 (d, 1H), 8.59 (m, 1H), 8.08 (d, 1H), 7.91 (d, 2H), 7.85 (m, 1H), 7.65 (m, 1H), 7.45 (m, 3H). MS (ESI) 298 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07087601B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-2b86ba7fc6984a3c8299ef5961aa3279 |
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| Quellennotiz | uspto-grants-2006_08 |
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