Réaction #7846

Équation de réaction

2-[4-(bromomethyl)-3-methoxyphenyl]-1,3-benzoxazole

chlorotrimethylsilane

2-bromopyridine

1,2-dibromoethane

→

2-[3-methoxy-4-(pyridin-2-ylmethyl)phenyl]-1,3-benzoxazole

Solvants

THF

Conditions de réaction

Traitement

1. 1
   TempératureThe mixture was heated
2. 2
   Températureat reflux for 1 h
3. 3
   FiltrationThe resultant organozinc reagent was filtered through a plug of Celite
4. 4
   Autretransferred to a flask
5. 5
   AutreThe mixture was degassed with bubbling argon for 15 min
6. 6
   Températureheated
7. 7
   Températureat reflux for 12 h
8. 8
   workup.ADDITIONThe reaction was poured into H2O (40 mL)
9. 9
   Extractionextracted with CH2Cl2 (2×30 mL)
10. 10
    SéchageThe organic extracts were dried (MgSO4)
11. 11
    Concentrationconcentrated
12. 12
    Autreto afford a colorless solid
13. 13
    AutrePurification of the solid by flash chromatography on silica gel (EtOAc:hexanes 3:1)

Mode opératoire

A solution of 2-[4-(bromomethyl)-3-methoxyphenyl]-1,3-benzoxazole (320 mg, 1.0 mmol) and THF (10 mL) was treated with Zn powder (activated by grinding with mortar and pestle), a drop of chlorotrimethylsilane, and a drop of 1,2-dibromoethane. The mixture was heated at reflux for 1 h. The resultant organozinc reagent was filtered through a plug of Celite, and transferred to a flask containing 2-bromopyridine (360 mg, 2.0 mmol) and Pd(Ph3P)4 (115 mg, 0.1 mmol). The mixture was degassed with bubbling argon for 15 min, and heated at reflux for 12 h. The reaction was poured into H2O (40 mL) and extracted with CH2Cl2 (2×30 mL). The organic extracts were dried (MgSO4) and concentrated to afford a colorless solid. Purification of the solid by flash chromatography on silica gel (EtOAc:hexanes 3:1) afforded the desired 2-[3-methoxy-4-(pyridin-2-ylmethyl)phenyl]-1,3-benzoxazole as a yellow solid: 1H NMR (CDCl3, 300 MHz) δ 8.55 (d, 1H), 7.76–7.82 (m, 3H), 7.56–7.62 (d, 2H), 7.32–7.36 (m, 3H), 7.11–7.16 (m, 2H), 4.23 (s, 2H), 3.95 (s, 3H). MS (ESI) 317 (M+H)+.

Source