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!

138505-27-8

4-bromo-1-isopropoxy-2-methoxybenzene synthesis

5synthesis methods
-

Yield:138505-27-8 100%

Reaction Conditions:

with potassium carbonate in N,N-dimethyl-formamide at 20 - 90;

Steps:

4.1.2. 4-(4-Isopropyloxy-3-methoxyphenyl)-3-butyn-1-ol (5b)

Isopropyl bromide (1.39 ml, 14.77 mmol) and anhydrous K2CO3 (2.04 g, 14.77 mmol) were added to a solution of 4-bromoguaiacol 4 (2.00 g, 9.85 mmol) in anhydrous DMF (10 ml). The mixture was stirred at 90 °C for 7 h, and then stirred at room temperature overnight, after which 100 ml of ethyl acetate and 100 ml of water were added. The two phases were separated and the aqueous phase was extracted again with 50 ml of ethyl acetate. The organic phases were pooled together and washed with 100 ml of HCl (0.05 M) and 100 ml of water. The organic phase was dried over anhydrous MgSO4, and the solvent was evaporated under reduced pressure. The crude compound was purified by flash column chromatography on silica gel (elution with 90/10 cyclohexane/ethyl acetate) to afford 2.43 g of isopropyl-bromoguaiacol in quantitative yield.

References:

Rivaud;Mendoza;Sauvain;Valentin;Jullian [Bioorganic and Medicinal Chemistry,2012,vol. 20,# 15,p. 4856 - 4861] Location in patent:experimental part