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ChemicalBook CAS DataBase List 3,4-DICHLOROPICOLINAMIDE
1025720-99-3

3,4-DICHLOROPICOLINAMIDE synthesis

6synthesis methods
3,4-dichloropicolinonitrile

1346167-25-6
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3,4-DICHLOROPICOLINAMIDE

1025720-99-3
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Yield:1025720-99-3 97%

Reaction Conditions:

with Acetaldehyde oxime;copper(II) oxide in water; for 2 h;Reflux;

Steps:

Experimental Procedures for Hydration of Various Nitriles

General procedure: To a 25 mL round-bottom flask equipped with magnetic stirrer were added nitrile (2.5 mmol), acetaldoxime (3.75 mmol), copper oxide (0.25 mmol) and H2O (10 mL). The mixture was heated to reflux for 2-14 h. After cooling to room temperature, the solution was directly evaporated to dryness and the residue was purified by column chromatography on silica gel (ethyl acetate/n-hexane) to give the corresponding amides. The commercially available amides were characterised by melting points, 2-amino-5-bromobenzamide (Table 2, entry 6) and 3,4-dichloropicolinamide (Table 2, entry 13) were characterised by NMR spectra and LC-MS.

References:

Ma, Xiao-Yun;He, Ying;Hu, Yu-Lin;Lu, Ming [Tetrahedron Letters,2012,vol. 53,# 4,p. 449 - 452] Location in patent:supporting information; experimental part

24424-99-5 Synthesis
Di-tert-butyl dicarbonate

24424-99-5
871 suppliers
$13.50/25G

959578-03-1 Synthesis
3,4-DICHLOROPICOLINIC ACID

959578-03-1
63 suppliers
$50.00/100mg

3,4-DICHLOROPICOLINAMIDE

1025720-99-3
30 suppliers
inquiry