Reacción #81037

ord-7550570bd5e147f9a251ee4012531873

Ecuación de reacción

O=C(O)c1cccc(O)c1
3-hydroxybenzoic acid
OCCCl
2-chloroethanol
O=C(OCCCl)c1cccc(O)c1
product
Rendimiento 95.2%
O=C(OCCCl)c1cccc(O)c1
2-Chloroethyl 3-hydroxybenzoate
Rendimiento 95.2%

Reactivos

Ninguno

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe excess chloroethanol was removed by evaporation
  2. 2
    Otroto obtain a brown solution which
  3. 3
    Lavadowashed with water
  4. 4
    SecadoThe organic layer was dried with MgSO4
  5. 5
    Concentraciónconcentrated

Procedimiento

A solution of 3-hydroxybenzoic acid (15.0 g, 0.11 mol) in 2-chloroethanol (70 mL, 1.0 mol) and 1 mL of concentrated sulfuric acid was refluxed for overnight. TLC analysis (silica gel/20% ethyl acetate/hexane) showed clean conversion to a new material. The excess chloroethanol was removed by evaporation to obtain a brown solution which was dissolved in ethyl acetate and washed with water. The organic layer was dried with MgSO4 and concentrated to obtain 21.0 g of the product as a white solid: mp 50° C.; 1H NMR (CDCl3) δ 3.81 (t, 2H, J=5.9 MHz), 4.57 (t, 2H, J=5.9 MHz), 4.77 (s, 1H), 7.06-7.66 (m, 4H); 13C NMR (CDCl3) δ 41.52, 64.75, 116.43, 120.77, 121.98, 129.80, 130.71,156.04, 166.57; MS m/e (tel intensity) 200 (26), 138 (59), 121 (100), 93 (31), 65 (21), 39 (12); Exact mass: calcd 200.0240, found 200.0242. ##STR28##

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05616729uspto-grants-1997_04