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ChemicalBook CAS DataBase List Methyl 2,6-dichloro-4-cyanobenzoate
409127-32-8

Methyl 2,6-dichloro-4-cyanobenzoate synthesis

5synthesis methods
methyl 4-carbamoyl-2,6-dichlorobenzoate

409127-31-7

Methyl 2,6-dichloro-4-cyanobenzoate

409127-32-8

Step a: Synthesis of methyl 2,6-dichloro-4-cyanobenzoate Methyl 4-carbamoyl-2,6-dichlorobenzoate (100 mg, 0.4 mmol) was dissolved in pyridine (2 mL) and trifluoroacetic anhydride (0.11 mL, 0.8 mmol) was added slowly and dropwise at 0 °C. The reaction mixture was gradually warmed to room temperature and stirred continuously for 1 hour. Upon completion of the reaction, the mixture was poured into pre-cooled ice water, the precipitated solid was filtered, washed thoroughly with cold water and dried to afford methyl 2,6-dichloro-4-cyanobenzoate (55 mg, 88% yield) as an off-white solid.

methyl 4-carbamoyl-2,6-dichlorobenzoate

409127-31-7
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Methyl 2,6-dichloro-4-cyanobenzoate

409127-32-8
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Yield:409127-32-8 88%

Reaction Conditions:

with pyridine;trifluoroacetic anhydride at 0 - 20; for 1 h;

Steps:



Step a: Synthesis of methyl 2,6-dichloro-4-cyanobenzoateTo a solution of methyl 4-carbamoyl-2,6-dichlorobenzoate (100 mg, 0.4 mmol) in pyridine (2 mL) trifluoro-acetic anhydride (0.1 1 ml, 0.8 mmol) was added drop wise at 0 °C. The reaction mixture was allowed to warm to room temperature and stirred for 1 hour. The contents were poured into ice cold water and the precipitated solid was filtered, washed with water and dried to yield methyl 2,6-dichloro-4- cyanobenzoate (55 mg, 88%) as an off-white solid.

References:

WO2012/160464,2012,A1 Location in patent:Page/Page column 77-78

264276-14-4 Synthesis
dimethyl 2,6-dichlorobenzene-1,4-dioate

264276-14-4
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Methyl 2,6-dichloro-4-cyanobenzoate

409127-32-8
57 suppliers
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