午夜插插,噜噜噜影院,啪啪伊人网,欧美熟夫,景甜吻戏视频,男人强操性感蕾丝美女视频在线网站,日本美女跳舞视频

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 tert-butyl 4-(2-hydroxyethyl)-3-oxopiperazine-1-carboxylate
910573-06-7

tert-butyl 4-(2-hydroxyethyl)-3-oxopiperazine-1-carboxylate synthesis

2synthesis methods
-

Yield:910573-06-7 998 mg

Reaction Conditions:

with tetrabutyl ammonium fluoride in acetonitrile at 40;

Steps:

109.1 Step 1: Synthesis of tert-butyl 4-(2-hydroxyethyl)-3-oxopiperazine-1-carboxylate

At room temperature, compounds 59-2 (1.50g, 4.18mmol) and tetrabutylammonium fluoride (3.50g, 20.9mmol) were sequentially added to acetonitrile (20.0mL) and reacted at 40 °C for 15h. TLC monitors reaction endpoints. The reaction solution was concentrated under reduced pressure, the residue was diluted with water (100mL), dichloromethane (50ml x 3) was extracted, the organic phase was combined, dried by anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure. The crude product was purified by rapid silica gel column chromatography (dichloromethane: methanol=99:1~20:1) to obtain the title product (998mg, colorless oil).

References:

WO2023/16521,2023,A1 Location in patent:Page/Page column 124