Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

2,3-dihydro-1,4-benzodioxine -6-carboxamide synthesis

3synthesis methods
-

Yield:299169-62-3 74%

Reaction Conditions:

Stage #1: 2,3-dihydrobenzo[b][1,4]dioxine-6-carbonitrilewith sulfuric acid;trifluoroacetic acid for 5 h;Reflux;
Stage #2: with waterCooling with ice;

Steps:

Transformations of benzonitriles 7c, 7d, 8, and 10 in CF3COOH-H2SO4 (general procedure).

General procedure: A solution of 3.5 mmol of 7c, 7d, 8, or 10 in a mixture of 1 mL of concentrated sulfuric acid and 4 mL of trifluoroacetic acid was refluxed for 5 h. The mixture was poured into a mixture of 35 mL of water and 35 g of ice, and the precipitate was filtered off, washed with water, and dried in air. If necessary, the product was recrystallized from an appropriate solvent. Compound 11 was described previously [17]. The yields of 13b and 13c are given in Table 1.

References:

Mochalov;Fedotov;Trofimova;Zefirov [Russian Journal of Organic Chemistry,2018,vol. 54,# 3,p. 403 - 413][Zh. Org. Khim.,2018,vol. 54,# 3,p. 399 - 408,10]