Реакция #9055

ord-bf56584023f540c7948984614ab8fea3

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Промывкаwashed consecutively with saturated aqueous NaHCO3 (40 mL) and H2O (40 mL)
  2. 2
    СушкаThe combined organic extracts were dried over MgSO4
  3. 3
    Концентрированиеconcentrated to a rusty brown solid (1.07 g, 97%)

Методика

To a stirred solution of 2,3-diaminotoluene (1.00 g, 8.2 mmol) in CH2Cl2 (82 mL) was added trimethylorthoformate (4.5 mL, 41 mmol) and trifluoroacetic acid (0.32 mL, 4.1 mmol) and the mixture stirred at room temperature for 24 h after which the reaction mixture was diluted with CH2Cl2 (200 mL), and washed consecutively with saturated aqueous NaHCO3 (40 mL) and H2O (40 mL). The aqueous layers were reextracted with CH2Cl2 (2×100 mL). The combined organic extracts were dried over MgSO4 and concentrated to a rusty brown solid (1.07 g, 97%). 1H NMR (300 MHz, CDCl3) δ 8.08 (s, 1H), 7.49 (d, 1H, J=8.1 Hz), 7.23–7.18 (m, 1H), 7.10 (d, 1H, J=7.5 Hz), 2.64 (s, 3H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07091217B2uspto-grants-2006_08