Extended knowledge of 5-Nitroindoline

The synthetic route of 32692-19-6 has been constantly updated, and we look forward to future research findings.

In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. 32692-19-6, name is 5-Nitroindoline belongs to indolines-derivatives compound, it is a common compound, a new synthetic route is introduced below. HPLC of Formula: C8H8N2O2

To a solution of 5-nitroindoline (11.72 g) and triethylamine (8.67 g) in N, N-dimethylformamide (150 ml) was added dropwise chloroacetyl chloride (8.06 g) at 5C and the mixture was stirred at ambient temperature for 20 hours. The mixture was poured into a mixture of ethyl acetate and water and the separated organic layer was washed with water and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was triturated with ethyl acetate and collected by filtration to give 1- (CHLOROACETYL)-5-NITROINDOLINE (14.66 g) as a yellow crystal. 1H-NMR (DMSO-d6): 8 3. 28 (2H, t, J=8.6 Hz), 4.25 (2H, t, J=8.6 HZ), 4.64 (2H, s), 8.1-8. 2 (3H, m) ESI-MS (m/z): 263 (M+Na) +

The synthetic route of 32692-19-6 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; FUJISAWA PHARMACEUTICAL CO., LTD.; DAISO CO., LTD.; WO2004/39795; (2004); A2;,
Indoline – Wikipedia,
Indoline | C8H9N – PubChem