天堂网亚洲,天天操天天搞,91视频高清,菠萝蜜视频在线观看入口,美女视频性感美女视频,95丝袜美女视频国产,超高清美女视频图片

Welcome to chemicalbook!
Chinese English Japanese Germany Korea
010-86108875
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 4-Morpholinopiperidine
53617-35-9

4-Morpholinopiperidine synthesis

9synthesis methods
4-(1-benzyl-piperidin-4-yl)-morpholine

415967-79-2

4-Morpholinopiperidine

53617-35-9

General procedure for the synthesis of 4-(4-piperidinyl)morpholine from N-benzyl-4-(4-morpholinyl)piperidine: 41.59 g (0.16 mol) of N-benzyl-4-(4-morpholinyl)piperidine was dissolved in 400 mL of methanol, and 5.2 g of 10% palladium/carbon catalyst was added. The hydrogenation reaction was carried out at room temperature for 18 hours at 50 psi hydrogen pressure. Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated. A colorless oily substance was obtained, which was left to crystallize. The yield was 25.29 g with 93% yield.

-

Yield:53617-35-9 100%

Reaction Conditions:

with palladium on activated charcoal;hydrogen in isopropyl alcohol at 80; under 3750.38 Torr; for 7 h;Autoclave;Reagent/catalyst;

Steps:

11 Example 11

The compound (3) (120 g; 0.46 mol), 2-propanol (276 g), and the palladium/carbon catalyst (0.3 g in terms of metallic palladium) were placed in an autoclave with a capacity of 1 L, and then the whole was stirred at 80° C., under a hydrogen pressure of 0.5 MPa for 7 hours. After cooling the reaction, the catalyst was filtered and washed with 2-propanol to obtain a filtrate. The resulting filtrate was analyzed by gas chromatography. As a result, the yield of the compound (4) analyzed by the internal standard method was 97%, and the area percentage (excluding the solvent and the compounds with low boiling points) of the compound (4) was 100% (Table 2).

References:

US2019/210968,2019,A1 Location in patent:Paragraph 0093

4-Morpholinopiperidine Related Search: