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ChemicalBook CAS DataBase List 2-ethyoxyl-4-broMobenzonitrile
1255870-63-3

2-ethyoxyl-4-broMobenzonitrile synthesis

3synthesis methods
Iodoethane

75-03-6

4-fluoro-2-hydroxybenzonitrile

186590-01-2

2-ethyoxyl-4-broMobenzonitrile

1255870-63-3

General procedure for the synthesis of 2-ethoxy-4-bromobenzonitrile from 4-fluoro-2-hydroxybenzonitrile and iodoethane: 4-fluoro-2-hydroxybenzonitrile (50 mg, 0.32 mmol) was dissolved in N,N-dimethylformamide (DMF, 2 mL) in a round-bottomed flask and finely ground potassium carbonate (133 mg, 0.96 mmol) was added under stirring conditions. Subsequently, ethidium iodide (0.03 mL, 0.39 mmol) was slowly added dropwise to the reaction mixture. The reaction process was monitored by thin layer chromatography (TLC) until the feedstock completely disappeared. Upon completion of the reaction, the DMF solvent was removed by distillation under reduced pressure. The residue was dissolved in ethyl acetate and subsequently washed with saturated saline. The organic phase was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography with the eluent ratio of petroleum ether: ethyl acetate = 5:1 to give 2-ethoxy-4-bromobenzonitrile (53.8 mg, 94% yield).

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Yield:1255870-63-3 94%

Reaction Conditions:

with potassium carbonate in N,N-dimethyl-formamide;

Steps:

43 (Experimental Method 1) 2-Ethoxy-4-bromo-benzonitrile

4-fluoro-2-hydroxybenzonitrile (50 mg, 0.32 mmol) and DMF (2 ml) were put in a round-bottom flask and stirred, finely ground potassium carbonate (133 mg, 0.96 mmol) was added thereto, and then iodoethane (0.03 ml, 0.39 mmol) was added thereto, followed by stirring.
After confirming by TLC that the base compound had disappeared, DMF was vacuum-distilled, and the residue was diluted with ethyl acetate and then washed with brine.
The residue obtained after vacuum distillation was subjected to column chromatography (hexane:ethyl acetate=5:1) to obtain 2-ethoxy-4-bromo-benzonitrile (53.8 mg).
(Yield: 94%)

References:

US2018/265462,2018,A1 Location in patent:Paragraph 0151