Reaction of hydroxyiminoacetophenone with p-toluenesulfonyl chloride and an X-ray diffraction study of the reaction product

DOI: 10.1007/BF02495228

Source and publish data:

Russian Chemical Bulletin p. 838 - 840 (1997)

Update date:2022-08-17

Topics:

Authors:

Fedorov Fedorov

Nesterov

Shestopalo

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1007/BF02495228

2-Benzoyloxy-2-phenylmalononitrile is formed instead of the expected oxime tosylate in the reaction of hydroxyiminoacetophenone with p-toluenesulfonyl chloride. The structure of the product was confirmed unambiguously by X-ray diffraction analysis.

Full text of DOI:10.1007/BF02495228

Products guided by the article

Product name:alpha,alpha-dicyanobenzyl benzoate

Cas No:5467-94-7

R&D Labs maybe for 5467-94-7

Zhejiang Kaili Industrial Co., Ltd

Contact:+86-571-85241926

Address:lantian business center,No.18 Moganshan Road
Quzhou Ruiyuan chemical Co., Ltd

Contact:+86-570-3039321/3039361/3039308

Address:18# Huayang Road,Quzhou High-tech Industrial Park, Zhejiang China.
Jiangsu Jiuri Chemical Co.,Ltd.

Contact:+86-519-82118868

Address:Tianwang Town, Jurong City, Jiangsu Province, China
ChangZhou Mascotchem. Co.,Ltd.

website:http://www.mascotchem.com

Contact:86-519-85010339

Address:B-802,XingBei Building,391#,Tongjiang Middle Road New District,Changzhou,JS,China
Ningxia Soochow Agrochemical Limited Company

Contact:(+86）0512 6320 8190

Address:wujiang

Relevant to this article

Mechanosynthesis of N-methyl imines using recyclable imidazole-based acid-scavenger: In situ formed ionic liquid as catalyst and dehydrating agent

Doi:10.1071/CH18408
(2019)
Rutinosidase from Aspergillus niger: crystal structure and insight into the enzymatic activity

Doi:10.1111/febs.15208
(2020)
Doi:10.1007/BF00526283
(1969)
Radiosynthesis and preliminary evaluation of ¹¹C-labeled 4-cyclopropyl-7-(3-methoxyphenoxy)-3,4-dihydro-2H-benzo[e] [1,2,4] thiadiazine 1,1-dioxide for PET imaging AMPA receptors

Doi:10.1016/j.tetlet.2020.151635
(2020)
Doi:10.1021/ja01279a030
(1938)
In situ formed acetals facilitated direct Michael addition of unactivated ketones

Doi:10.1039/C6NJ02954J
(2017)

Article Doi