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 N-(tert-Butoxycarbonyl)-4-piperidone
79099-07-3

N-(tert-Butoxycarbonyl)-4-piperidone synthesis

13synthesis methods
24424-99-5 Synthesis
Di-tert-butyl dicarbonate

24424-99-5
834 suppliers
$13.50/25G

41979-39-9 Synthesis
4-oxopiperidinium chloride

41979-39-9
114 suppliers
$15.00/10mg

-

Yield:79099-07-3 100%

Reaction Conditions:

Stage #1: di-tert-butyl dicarbonate;4-piperidone hydrochloridewith triethylamine;dmap in methanol at 20; for 20 h;
Stage #2: with hydrogenchloride in dichloromethane;

Steps:

8

Triethylamine (19.2g, 190mmol) was added to a stirring solution of 4-piperidone monohydrate hydrochloride (20.0g, 131mmol) in methanol (300mL) and stirred for 5min. Boc20 (34g, 168mmol) was added in portions over a 5min period, followed by DMAP (0.4g, 3mmol). The solution was stirred at ambient temperature for 20h. The methanol was removed under reduced pressure and the crude was dissolved in dichloromethane (100mL). The organic phase was washed with HCI (2M, 2 x 70mL) sat. Na2C03 (70mL) and sat NaCI (50mL), dried over Na2S04, filtered and evaporated to dryness to yield 1- Boc-4-piperidone as a white solid in quantitative yield. 1H NMR (CDCI 3400m Hz) δ 3.71 (t, J=6.2Hz, 4H), 2.44 (t, J=6.2Hz, 4H), 1.49 (s, 9H).

References:

WO2012/142668,2012,A1 Location in patent:Page/Page column 50; 51

N-(tert-Butoxycarbonyl)-4-piperidone Related Search: