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!

ChemicalBook CAS DataBase List Tetracyanoethylene
670-54-2

Tetracyanoethylene synthesis

7synthesis methods
-

Yield:670-54-2 37%

Reaction Conditions:

with selenium(IV) oxide in toluene at 100; for 1.25 h;

Steps:

Tetracyanoethylene (1).
Malononitrile, 6.61 g(0.1 mol), and selenium (IV) oxide, 16.65 g (0.15 mol),were added in succession to 75 mL of freshly distilled anhydrous toluene. The mixture was heated with stirring to 100°C (glycerol bath) and was kept for 75 min at that temperature. The mixture gradually turned yellow and then brown and dark red. In some cases, a small amount of yellow smoke was observed. When the reaction was complete, the mixture was heated to 110°C and filtered while hot through a filter paper, the filtrate was cooled, and the solvent was distilled off. The residue was 3.46 g (54%) of a red-brown material which was sublimed twice under reduced pressure at 130-140°C. Yield 2.37 g (37%),white crystals, mp 200-202°C; published data [12]:mp 199-200°C. IR spectrum, ν, cm-1: 2262, 2228,2220 (CN). 13C NMR spectrum (acetone-d6), δC, ppm:107.8 (CN), 111.9 (C=C).

References:

Kachanov;Slabko, O. Yu.;Kaminskii [Russian Journal of Organic Chemistry,2017,vol. 53,# 3,p. 462 - 464][Zh. Org. Khim.,2017,vol. 53,# 3,p. 452 - 453,2]

FullText

Tetracyanoethylene Related Search: