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
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 (S)-(+)-4-Isopropyl-3-propionyl-2-oxazolidinone
77877-19-1

(S)-(+)-4-Isopropyl-3-propionyl-2-oxazolidinone synthesis

9synthesis methods
-

Yield: 99%

Reaction Conditions:

Stage #1:(4S)-4-isopropyl-1,3-oxazolidin-2-one with triethylamine;lithium chloride in tetrahydrofuran at 0; for 0.5 h;
Stage #2:propionic acid anhydride in tetrahydrofuran at 0 - 20; for 1.5 - 2 h;

Steps:

2
Example 2: Preparation of (S)-4-isopropyl-3-propionyloxazolidin-2-one (3) The compound (2) prepared in Example 1 (10Og) was dissolved in tetrahydrofuran (300mNo.), and cooled to 0°C . Lithium chloride (36g) was added, triethylamine (10Ig) was then slowly added, and the resulting mixture was stirred for 30 min. Propionic acid anhydride (106g) was slowly added over a 30 min. time period. The reaction mixture was slowly warmed to room temperature, and stirred for 1-1.5 h. The reaction solution was cooled, IN aqueous sodium chloride solution (300mNo.) was added, and the mixture was stirred for 30 min. Ethyl acetate (300mf) was added, the phases were separated, and extracted once again by ethyl acetate (300m£). After washing with 1.5 N hydrochloric acid (300m£), the organic phase was washed once again with aqueous sodium chloride solution (300mNo.), dried, filtered and distilled to produce the title compound (142g, Yield%). 1H NMR (300MHz, CDCl3) δ 4.4 (m, IH), 4.3-4.2 (m, 2H), 2.97 (m, 2H), 2.3 (m,IH), 1.2 (t, 3H), 0.93 (dd, 6H)

References:

DAEWOONG PHARMACEUTICAL CO., LTD.;DAEWOONG CHEMICAL CO., LTD. WO2008/127070, 2008, A1 Location in patent:Page/Page column 13-14

(S)-(+)-4-Isopropyl-3-propionyl-2-oxazolidinone Related Search: