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 Benzocaine
94-09-7

Benzocaine synthesis

11synthesis methods
Benzocaine is the ethyl ester of 4-aminobenzoic acid (2.3.1). The classic, optimal way of benzocaine synthesis is the reduction of the nitro group of the ethyl ester of 4-nitrobenzoic acid to benzocaine by hydrogen, which generates directly in the reaction medium by the reaction of iron filings with dilute acids [24–26].

-

Yield:94-09-7 100%

Reaction Conditions:

with hydrogen in methanol at 20; under 760.051 Torr; for 6 h;chemoselective reaction;Reagent/catalyst;

Steps:

4.4 General procedure for the hydrogenation

General procedure: A mixture of the substrate (0.250mmol) and catalyst [8% Pd/CR11 (3.3mg, 2.50μmol) or 9% Pd/CR20 (3.0mg, 2.50μmol)] in MeOH (1mL) was stirred under an H2 atmosphere (balloon) at room temperature. After a specific time, the mixture was filtered through a membrane filter (0.45 or 0.2μm), and the filtrate was concentrated in vacuo to give the corresponding spectrometrically-pure reduced product. If the reaction was not completed, the temperature was raised to 40 or 50°C. If the reaction was still incomplete, the H2 pressure was increased to 3 or 5atm. All the products were known, and the 1H NMR spectral data of the products were identical to those in the literature (see Supplementary data).

References:

Monguchi, Yasunari;Ichikawa, Tomohiro;Nozaki, Kei;Kihara, Kensuke;Yamada, Yuuko;Miyake, Yutaka;Sawama, Yoshinari;Sajiki, Hironao [Tetrahedron,2015,vol. 71,# 37,art. no. 26568,p. 6499 - 6505] Location in patent:supporting information

Benzocaine Related Search: