Reacción #725941

ord-b889b1a3d7314ea183a6f0d14413f00a

Ecuación de reacción

O=C(Cl)COCc1ccccc1
Benzyloxy acetyl chloride
COC(=O)C(C)c1ccc2cc(O)ccc2c1
2-(6-Hydroxynaphthalen-2-yl)-propionic acid methyl ester
CCN(CC)CC
triethylamine
COC(=O)C(C)c1ccc2cc(OC(=O)COCc3ccccc3)ccc2c1
99
Rendimiento 63.9%
COC(=O)C(C)c1ccc2cc(OC(=O)COCc3ccccc3)ccc2c1
2-[6-(2-Benzyloxyacetoxy)naphthalen-2-yl]propionic acid methyl ester
Rendimiento 63.9%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónSolids were filtered off
  2. 2
    workup.DISTILLATIONacetone distilled off
  3. 3
    workup.ADDITIONwater (100 ml) added
  4. 4
    ExtracciónCrude 99 was extracted into chloroform
  5. 5
    Lavadowashed with 5% sodium bicarbonate (2×50 ml), water (2×50 ml)
  6. 6
    Secadodried over sodium sulphate
  7. 7
    workup.DISTILLATIONdistilled
  8. 8
    OtroCrude 99 was purified
  9. 9
    Otroby recrystallising in chloroform:hexane (1:6)

Procedimiento

Benzyloxy acetyl chloride (24 gm, 86.95 mmol) was added drop-wise to a mixture of 2-(6-Hydroxynaphthalen-2-yl)-propionic acid methyl ester 6 (20 g, 86.95 mmol) and triethylamine (22.5 g, 222.35 mmol) in acetone (300 ml) and stirred for 2 hrs at room temp. Solids were filtered off, acetone distilled off, and water (100 ml) added. Crude 99 was extracted into chloroform, washed with 5% sodium bicarbonate (2×50 ml), water (2×50 ml), dried over sodium sulphate and distilled. Crude 99 was purified by recrystallising in chloroform:hexane (1:6) to get pure 99 (21 g, 63.9%) as a white powder. M.p: 58-60° C.

Fuente

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