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Methyl 4-Oxo-4,5,6,7-Tetrahydrobenzo[B]Thiophene-5-Carboxylate synthesis

3synthesis methods
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Yield:112101-60-7 125 mg

Reaction Conditions:

with sodium hydroxide at 85; for 3 h;Inert atmosphere;

Steps:

11a a) Methyl 4-oxo-4,5,6,7-tetrahydrobenzothiophene-5-carboxylate

Under nitrogen protection, 6,7-dihydrobenzothiophen-4(5H)-one (110 mg)Dissolved in dimethyl carbonate (5ml),Sodium hydrogen (35 mg, 60% w/w) was added in portions with stirring,The reaction was refluxed at 85°C for 3 hours. It was then cooled to 10°C, quenched by adding water (20 ml), and extracted by adding ethyl acetate (50 ml). The organic phase was concentrated to dryness, and the residue was subjected to silica gel column chromatography to obtain 125 mg of the title product.

References:

CN114380841,2022,A Location in patent:Paragraph 0171-0174