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ChemicalBook CAS DataBase List 4-(2,3-EPOXYPROPYL)MORPHOLINE
6270-19-5

4-(2,3-EPOXYPROPYL)MORPHOLINE synthesis

2synthesis methods
-

Yield: 88.8%

Reaction Conditions:

Stage #1:morpholine;epichlorohydrin in tert-butyl alcohol at 0 - 20;Cooling with ice-water;
Stage #2: with potassium tert-butylate in tetrahydrofuran;tert-butyl alcohol at 10;Cooling with ice-water;

Steps:

53.1
Step 1 4-Oxiranylmethyl-morpholine Morpholine 53a (8.712 ml, 0.1 mol) was dissolved in tert-butanol (4.5 ml) under stirring at room temperature, and (R)-(-)-1-chloro-2,3-epoxypropane (8.05 ml, 0.1 mol) was added slowly to the solution at 0° C. in an ice-water bath. Upon completion of the addition, the ice-water bath was removed, and the reaction mixture was allowed to warm up to room temperature and stirred for 24 hours. After thin lay chromatography showed the disappearance of starting materials, the reaction mixture was added dropwise with a solution of potassium tert-butoxide in tetrahydrofuran (60 ml, 1.67 mol/L, 100 mmol) while maintaining the temperature below 10° C. in an ice-water bath, gradually turned from light yellow to white turbid solution and stirred for 30 minutes. After thin lay chromatography showed the disappearance of starting materials, the reaction mixture was concentrated under reduced pressure, added with water (50 ml), exacted with dichloromethane (100 ml*2). The combined organic extracts were washed with saturated brine (100 ml), dried over anhydrous magnesium sulfate, filtered to remove the drying agent and concentrated under reduced pressure to obtain the title compound 4-oxiranylmethyl-morpholine 53b (12.7 g, yield 88.8%) as a yellow oil.

References:

ChoTang, Peng Cho;Su, Yidong;Li, Yali;Zhang, Lei;Zhao, Fuqiang;Yang, Jialiang;Zhou, Ying;Bie, Pingyan;Qian, Guangtao;Ju, Minggang US2010/75952, 2010, A1 Location in patent:Page/Page column 75

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