Reacción #725882

ord-41c10a4ce91a402cbb0b813d743c72d9

Ecuación de reacción

O=S(=O)(O)O
sulphuric acid
CC(C(=O)O)c1ccc2cc(O)ccc2c1
2-(6-Hydroxynaphthalen-2-yl)-propionic acid
CC(C(=O)O)c1ccc2cc(O)ccc2c1
2-(6-Hydroxynaphthalen-2-yl)propionic acid
CO
methanol
COC(=O)C(C)c1ccc2cc(O)ccc2c1
6
Rendimiento 89.5%
COC(=O)C(C)c1ccc2cc(O)ccc2c1
2-(6-Hydroxynaphthalen-2-yl)-propionic acid methyl ester
Rendimiento 89.5%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturarefluxed for 6 hours
  2. 2
    workup.DISTILLATIONMethanol (1000 ml) was distilled off
  3. 3
    Otrothe cooled reaction mass
  4. 4
    workup.ADDITIONwas poured onto ice water (3000 ml)
  5. 5
    FiltraciónCrude 6 was filtered
  6. 6
    Otrodried
  7. 7
    Otrorecrystallised from a mixture of ethyl acetate:hexane (1:5)

Procedimiento

To a solution of methanol (2100 ml) and sulphuric acid (84 ml) was added 2-(6-Hydroxynaphthalen-2-yl)-propionic acid 5 (420 g, 1.944 mmol), and refluxed for 6 hours. Methanol (1000 ml) was distilled off and the cooled reaction mass was poured onto ice water (3000 ml). Crude 6 was filtered, dried and recrystallised from a mixture of ethyl acetate:hexane (1:5) to give pure 6 (400 g, 89.5%) as a white fluffy powder. The melting point found to be 89.5-92° C. The structure was confirmed with IR and NMR.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07691364B2uspto-grants-2010_04