Reacción #819491

Ecuación de reacción

chloromethyl methyl ether

6-hydroxy coumarin

acetonitrile

chloromethyl methyl ether

N,N-diisopropylethylamine

→

6-methoxymethoxy coumarin

Rendimiento 50.7%

Disolventes

ethyl acetate heptane

Condiciones de reacción

Tratamiento posterior

1. 1
   Otrois used without further purification
2. 2
   OtroEquip a 2-L, three-neck, round-bottom flask with a magnetic stir bar
3. 3
   Otrothe temperature below 40° C
4. 4
   workup.STIRRINGStir at room temperature for 15 h
5. 5
   Otroquench the reaction mixture with saturated aqueous ammonium chloride (500 mL)
6. 6
   Extracciónextracted with ethyl acetate
7. 7
   Secadodry over anhydrous magnesium sulfate
8. 8
   Filtraciónfilter
9. 9
   Concentraciónconcentrate under reduced pressure
10. 10
    OtroPurify the residue by column chromatography on silica gel (30-50% ethyl acetate/heptane)
11. 11
    Otroto afford a light yellow solid
12. 12
    Filtraciónfilter
13. 13
    Otrodry

Procedimiento

Equip a 3-L, three-neck, round-bottom flask equipped with a large blade mechanical stirrer, a thermocouple, a Claisen adapter, an addition funnel, and a reflux condenser. Add 2,5-dimethoxycinnamic acid (102.8 g, 493 mmol, 1.0 equiv) and dichloroethane (1.5 L). Add boron tribromide (247.4 g, 987 mmol, 2.0 equiv) dropwise over 45 min while keeping the temperature below 40° C. Rapidly stir the resulting mixture and heat gradually to 83° C. over 45 min, monitoring the temperature increase and gas evolution. Stir for 6 h at reflux then for 15 h at 76° C. Cool the resulting mixture to room temperature and quenched carefully with water (450 mL). Filter the solid, wash with heptane and dry under vacuum to afford 6-hydroxy coumarin (95 g) as a light brown solid which is used without further purification. Equip a 2-L, three-neck, round-bottom flask with a magnetic stir bar and a thermocouple. Add 6-hydroxy coumarin (39.8 g, 245 mmol, 1.0 equiv), anhydrous acetonitrile (700 mL) and N,N-diisopropylethylamine (200 mL, 1.15 mol, 4.7 equiv). Add chloromethyl methyl ether (40.0 mL, 527 mmol, 2.1 equiv) dropwise over 30 min while keeping the temperature below 40° C. Stir the resulting mixture at room temperature for 3 h, then add an additional equiv of chloromethyl methyl ether. Stir at room temperature for 15 h, then quench the reaction mixture with saturated aqueous ammonium chloride (500 mL) and extracted with ethyl acetate. Combine the organic extracts and dry over anhydrous magnesium sulfate, filter and concentrate under reduced pressure. Purify the residue by column chromatography on silica gel (30-50% ethyl acetate/heptane) to afford a light yellow solid. Suspend the solid in a mixture of ethyl acetate/heptane (150 mL, 10:90), filter and dry to afford 6-methoxymethoxy coumarin 17a (25.6 g, 50%) as a white solid: 1H NMR (300 MHz, CDCl3) δ 7.70 (d, J=7.8 Hz, 1H), 7.30-7.12 (m, 3H), 6.41 (d, J=7.8 Hz, 1H), 5.20 (s, 2H), 3.48 (s, 3H); 13C NMR (75 MHz, CDCl3) δ 161.2, 154.0, 149.5, 143.5, 121.6, 119.6, 118.1, 117.3, 113.8, 95.3, 56.4; IR (KBr) 1714 (s), 1570 (s), 1491 (m), 1447 (m), 1266 (s), 1154 (s), 1070 (s), 1017 (s) cm−1; ESI MS m/z 207 [C11H10O4+H]+.

Fuente