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 MYOSMINE
532-12-7

MYOSMINE synthesis

10synthesis methods
-

Yield:532-12-7 77.2%

Reaction Conditions:

Stage #1:methyl 3-pyridinecarboxylate;1-(but-1-enyl) pyrrolidin-2-one with sodium hydride in N,N-dimethyl-formamide at 90; for 2 h;
Stage #2: with hydrogenchloride in water at 110; for 12 h;
Stage #3: with sodium hydroxide in water; pH=14 at 0;

Steps:

2
Sodium hydride (17.26 g, 072 mol of 60% dispersion in a mineral oil) was washed with toluene (25 ml x 2) to remove mineral oil and added to 25 ml of DMF. To this a solution containing 1-(but-1-enyl)-pyrrolidin-2-one (I, 50 g, 0.3597 mol) and methyl nicotinate (41.8 g, 0.3057 mol) in 50 ml of DMF was added. The reaction mixture was heated to 90°C for 2 hrs. DMF was partially removed under reduced pressure and 100 ml water and HCl (165 ml) were added. The reaction mixture was heated to 110°C for 12 hr, cooled and washed with ethyl acetate (50 ml x 2). The aqueous layer was cooled to 0°C, pH adjusted to about 14 using NaOH, extracted with dichloromethane (100 ml x 4), the extract dried over Na2SO4, the solvent removed completely and the crude solid was purified by high vacuum distillation to get myosmine (34.38 g, 77.2 % yield, 98.5% purity by GC).

References:

Divi's Laboratories Limited EP2487172, 2012, A1 Location in patent:Page/Page column 5

FullText

MYOSMINE Related Search: