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1-(2-Ethoxy-2-oxoethyl)pyridinium bromide

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1-(2-Ethoxy-2-oxoethyl)pyridinium bromide Basic information
Product Name:1-(2-Ethoxy-2-oxoethyl)pyridinium bromide
Synonyms:1-(2-Oxo-2-ethoxyethyl)pyridinium·bromide;1-(Ethoxycarbonylmethyl)pyridinium·bromide;Pyridinium-1-acetic acid ethyl·bromide;N-(ethoxycarbonylMethyl)-pyridiniuM broMide;1-(2-Ethoxy-2-oxoethyl)pyridin-1-iuM broMide;PyridiniuM, 1-(2-ethoxy-2-oxoethyl)-, broMide;1-(ethoxycarbonylmethyl)-pyridiniubromide;1-amino-4-(3-ethenylsulfonylanilino)-9,10-dioxo-2-anthracenesulfonic acid
CAS:17282-40-5
MF:C9H12BrNO2
MW:246.1
EINECS:
Product Categories:
Mol File:17282-40-5.mol
1-(2-Ethoxy-2-oxoethyl)pyridinium bromide Structure
1-(2-Ethoxy-2-oxoethyl)pyridinium bromide Chemical Properties
Melting point 137-139°C
storage temp. Inert atmosphere,Room Temperature
AppearanceWhite to off-white Solid
Safety Information
HazardClass IRRITANT
Toxicitymouse,LDLo,subcutaneous,370mg/kg (370mg/kg),Journal of Pharmacology and Experimental Therapeutics. Vol. 35, Pg. 75, 1929.
MSDS Information
1-(2-Ethoxy-2-oxoethyl)pyridinium bromide Usage And Synthesis
Synthesis
Pyridine

110-86-1

Ethyl bromoacetate

105-36-2

1-(2-ETHOXY-2-OXOETHYL)PYRIDINIUM BROMIDE

17282-40-5

Example 3: Synthesis of compounds shown in chemical formula 11 According to reaction scheme 3, the steps for the synthesis of the compound shown in chemical formula 11 are as follows: Step 1: Synthesis of intermediate G 105.0 g (628.4 mmol) of ethyl bromoacetate and 994.67 g (12.6 mol) of pyridine were suspended in an appropriate amount of solvent. The suspension was stirred and reacted at room temperature for 2 hours. Upon completion of the reaction, 1,000 mL of diethyl ether was added to the reaction mixture to induce precipitation of the product. The precipitated pale yellow solid was separated by filtration and washed with diethyl ether. After drying, 152.3 g of Intermediate G was obtained in 98% yield.

References[1] Patent: US2012/313091, 2012, A1. Location in patent: Page/Page column 69-70
[2] Journal of the American Chemical Society, 1981, vol. 103, # 11, p. 3233 - 3235
[3] European Journal of Organic Chemistry, 2015, vol. 2015, # 13, p. 2889 - 2901
[4] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1981, p. 1180 - 1185
[5] Journal of Materials Chemistry, 1999, vol. 9, # 9, p. 2183 - 2188
1-(2-Ethoxy-2-oxoethyl)pyridinium bromide Preparation Products And Raw materials
Raw materialsPyridine-->Ethyl bromoacetate
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