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HRID 2164056作成日:2026年10月27日

Hydrochloric Acid → 4-(9,10-dihydro-4-oxo-4H-benzo[4,5]cyclohepta[1,2-b]thiophen-2-yl)-4-oxobutyric acid methyl ester

https://huagongshe.com/reaction/2164056

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Tin tetrachlorideHCID 24287—
反応物9,10-Dihydro-4H-benzo[4,5]cyclohepta[1,2-b]thiophen-4-oneHCID 768492—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物Succinic acid methylester chlorideHCID 86605420—
溶媒Carbon DisulfideHCID 6348—
生成物4-(9,10-dihydro-4-oxo-4H-benzo[4,5]cyclohepta[1,2-b]thiophen-2-yl)-4-oxobutyric acid methyl esterHCID 53750201—

反応手順

A solution of 6.3 cc of succinic acid monomethyl ester chloride in 100 cc of anhydrous carbon disulphide is added dropwise at 0° to a suspension of 10.0 g of 9,10-dihydro-4H-benzo[4,5]cyclohepta[1,2-b]thiophen-4-one and 30.0 g of anhydrous aluminium chloride in 200 cc of anhydrous carbon disulphide, the reaction mixture is stirred for a further 6 hours at room temperature, 23.3 g of tin tetrachloride are added dropwise thereto at 20° to 25° and stirring is continued at room temperature for 15 hours. The reaction mixture is subsequently heated to 50° for 2 hours, cooled, poured on 500 cc of 5 N hydrochloric acid and extracted with chloroform. The organic phases are washed with 5 N hydrochloric acid and with water, dried over magnesium sulphate and concentrated by evaporation. The evaporation residue is dissolved in 300 cc of methylene chloride, filtered through silica gel and evaporated to dryness. The title compound crystallizes from benzene/petroleum ether and is recrystallized once from ether. M.P. 97°-98°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04137323
出典データセットuspto-grants-1979_01
ORD IDord-6405bb5f8efd47b98612727ab016bef0
出典メモuspto-grants-1979_01