Реакция #433765

ord-6d6648e82c574ae48b32403967abf004

Уравнение реакции

O=C(Cl)OC(Cl)(Cl)Cl
Trichloromethyl chloroformate
Cc1ccc(N)c(C(=O)O)c1
Compound 10
Cc1ccc(N)c(C(=O)O)c1
2-Amino-5-methyl benzoic acid
Cc1ccc2[nH]c(=O)oc(=O)c2c1
white solids
Выход 94.1%
Cc1ccc2[nH]c(=O)oc(=O)c2c1
6-Methyl-1H-benzo[d][1,3]oxazine-2,4-dione
Выход 94.1%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураthe solution was refluxed for 4 h
  2. 2
    ТемператураThe solution was cooled in ice bath
  3. 3
    Другоеthe solids formed
  4. 4
    Фильтрацияwere filtered
  5. 5
    ПромывкаThe solids were washed by ether
  6. 6
    Другоеdried under vacuum at room temperature

Методика

Trichloromethyl chloroformate (36.27 mL, 300 mmol) was added to a stirred solution of Compound 10 (41.3 g, 273 mmol) in dry dioxane at room temperature and the solution was refluxed for 4 h. The solution was cooled in ice bath and the solids formed were filtered. The solids were washed by ether and dried under vacuum at room temperature to yield 45.5 g (94%) of white solids. M.P. 257° C. 1H NMR (DMSO-d6): δ 2.32 (s, 3H), 7.06 (d, J=8.6 Hz, 1H), 7.56 (dd, J=8.6, 1.8 Hz, 1H), 7.71 (d, J=1.1, 1H), 11.63 (s, 1H). EIMS (neg. mode) m/z 176 (M−1), 152 (M+23). Anal. (C9H7NO3) C, H, N.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07173036B2uspto-grants-2007_02