成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

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!

600-20-4

2-Butanone, 3-methyl-, oxime synthesis

3synthesis methods
-

Yield:1118-69-0 67% ,600-20-4 10%

Reaction Conditions:

with acetylhydroxamic acid;sulfuric acid in acetonitrile; for 9.5 h;Reflux;

Steps:

Typical procedure for the preparation of amide under conventional heating:

General procedure: Acetophenone 1a (1.0 g, 8.3 mmol), acetohydroxamic acid (0.92 g, 12.5 mmol), acetonitrile (10 ml), and conc. H2SO4 (0.2 ml) were taken into a 25 ml round bottomed flask fitted with a condenser and calcium chloride guard tube. The mixture was refluxed and the progress of the reaction was monitored by tlc. After completion of the reaction (8.5 h), the reaction mixture was cooled to room temperature and diluted with ethyl acetate (5 ml). Next, saturated sodium bicarbonate solution (10 ml) was added drop-wise to the mixture for the neutralization of sulfuric acid and then extracted with ethyl acetate (2 × 10 ml). The combined organic layer was washed with saturated NaCl solution, dried over anhy. Na2SO4, and concentrated under reduced pressure. The crude product was purified by normal column chromatography (silica gel 60-120 mesh, ethyl acetate/hexane: 1:4) to obtain acetanilide 2a (0.89 g, 80%, mp 114-116 °C) and acetophenone oxime 3a (76 mg, 7%, mp 55-60 °C) in the form of white powders.

References:

Madabhushi, Sridhar;Chinthala, Narsaiah;Vangipuram, Venkata Sairam;Godala, Kondal Reddy;Jillella, Raveendra;Mallu, Kishore Kumar Reddy;Beeram, China Ramanaiah [Tetrahedron Letters,2011,vol. 52,# 46,p. 6103 - 6107] Location in patent:experimental part