Реакция #1256754

ord-2e8cf1b99dc94740a5a31248a9f44c7a

Уравнение реакции

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

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe pyridine was removed under vacuum
  2. 2
    workup.DISSOLUTIONthe residue dissolved in ethyl acetate (50 ml)
  3. 3
    ПромывкаThis solution was washed with 1M HCl (10 ml) and brine (5 ml)
  4. 4
    Сушкаdried (MgSO4)
  5. 5
    Другоеthe solvent removed in vacuo
  6. 6
    Другоеto afford a pale orange oily solid
  7. 7
    ДругоеRecrystallisation from hexane

Методика

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+).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07825113B2uspto-grants-2010_11