Reacción #1256754

ord-2e8cf1b99dc94740a5a31248a9f44c7a

Ecuación de reacción

Cc1ccc(N)c(C(=O)O)c1
2-amino-5-methylbenzoic acid
CCCCCCCCOC(=O)Cl
octyl chloroformate
CCCCCCCCOc1nc2ccc(C)cc2c(=O)o1
desired product
Rendimiento 25.0%
CCCCCCCCOc1nc2ccc(C)cc2c(=O)o1
6-Methyl-2-octyloxy-4H-3,1-benzoxazin-4-one
Rendimiento 25.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe pyridine was removed under vacuum
  2. 2
    workup.DISSOLUTIONthe residue dissolved in ethyl acetate (50 ml)
  3. 3
    LavadoThis solution was washed with 1M HCl (10 ml) and brine (5 ml)
  4. 4
    Secadodried (MgSO4)
  5. 5
    Otrothe solvent removed in vacuo
  6. 6
    Otroto afford a pale orange oily solid
  7. 7
    OtroRecrystallisation from hexane

Procedimiento

A solution of 2-amino-5-methylbenzoic acid (302 mg, 2 mmol) in pyridine (10 ml) was cooled to 0° C. and treated dropwise with octyl chloroformate (1.15 ml, 6 mmol). The resulting mixture was allowed to warm to room temperature and stirred for 4 h. The pyridine was removed under vacuum and the residue dissolved in ethyl acetate (50 ml). This solution was washed with 1M HCl (10 ml) and brine (5 ml), dried (MgSO4) and the solvent removed in vacuo to afford a pale orange oily solid. Recrystallisation from hexane afforded the desired product as an off-white solid (144 mg, 25%); δH (400 MHz, DMSO-d6) 0.68 (3H, t, J 7, CH2CH3), 1.26-1.40 (10H, m, 5×CH2), 1.73 (2H, tt, J. J′ 7, OCH2CH2), 2.35 (3H, s, CH3), 4.35 (2H, t, J 7, OCH2), 7.34 (1H, d, J 8, Ph), 7.65 (1H, d, J 8, Ph), 7.83 (1H, s, Ph); m/z (ES+) 290 (MH+).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07825113B2uspto-grants-2010_11