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HRID 1242作成日:2026年10月25日

Benzoyl Peroxide → Ethyl 4-[(5,6,7,8-tetrahydro-8,8-dimethyl-5-thioacetylnaphth-2-yl)ethynyl]benzoate

https://huagongshe.com/reaction/1242

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl PeroxideHCID 7187—
反応物N-bromobutanimideHCID 67184—
反応物Ethyl 4-[(5,6,7,8-tetrahydro-8,8-dimethylnaphth-2-yl)ethynyl]benzoateHCID 19694975—
反応物Potassium ethanethioateHCID 23670855—
溶媒Carbon TetrachlorideHCID 5943—
生成物Ethyl 4-[(5,6,7,8-tetrahydro-8,8-dimethyl-5-thioacetylnaphth-2-yl)ethynyl]benzoateHCID 19694969—

反応手順

To a solution of 543 mg (1.64 mmol) of ethyl 4-[(5,6,7,8-tetrahydro-8,8-dimethylnaphth-2-yl)ethynyl]benzoate (obtainable from Compound M by coupling with ethyl-4-iodobenzoate) in 20 ml of CCl4 was added 320 mg (1.81 mmol) of N-bromosuccinimide and 26 mg (0.11 mmol) of benzoyl peroxide. The mixture was refluxed for 3 hours under argon atmosphere, cooled, filtered through celite and concentrated in vacuo to a dark brown syrup. The syrup was taken up in 20 ml of dry THF and 780 mg (6.9 mmol) of potassium thioacetate was added. The mixture was refluxed for 4 hours under argon atmosphere, concentrated in vacuo and purified by chromatography (silica, 10% EtOAc-hexane) to yield the title compound as a pale yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723620
出典データセットuspto-grants-1998_03
ORD IDord-a56f7e2293dc4862a8c854ae1b1ae4b3
出典メモuspto-grants-1998_03