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!

68301-49-5

ETHYL 2-AMINO-4-P-TOLYLTHIAZOLE-5-CARBOXYLATE synthesis

1synthesis methods
-

Yield:68301-49-5 41%

Reaction Conditions:

with ammonium iodide;lithium perchlorate;Alanine in water;dimethyl sulfoxide at 30;Electrolysis;

Steps:

General procedure for the one-pot electrochemically synthesis of 2-aminothiazoles from active methylene ketones and thioureas

General procedure: A 50 mL undivided cell was equipped with a graphite plate cathode and a graphiteplate anode (each about 2 × 2 cm2) which were connected to a DC regulated powersupply. To the cell was added active methylene ketone 1 (2 mmol), thiourea 2 (1 mmol),NH4I (0.1 mmol), DL-alanine (1 mmol) and LiClO4 (0.5 mmol) dissolved in a mixedsolvent of DMSO (1 mL) and H2O (14 mL). The mixture was electrolyzed underconstant current conditions at 5 mA/cm2 at 30 °C while stirring. The electrolysis wasterminated when 6 F/mol of charge had been consumed. After the electrolysis, thereaction mixture was washed with a saturated aqueous Na2S2O3 and the product wasthen extracted with DCM (3 × 10 mL), dried over MgSO4, and concentrated in vacuum.The residue was purified by column chromatography on silica gel using a mixture ofpetroleum ether/EtOAc as eluent.

References:

Yang, Shang-Feng;Li, Pei;Fang, Zi-Lin;Liang, Sen;Tian, Hong-Yu;Sun, Bao-Guo;Xu, Kun;Zeng, Cheng-Chu [Beilstein Journal of Organic Chemistry,2022,vol. 18,p. 1249 - 1255] Location in patent:supporting information