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HRID 982049作成日:2026年10月24日

Diethyl [chloro(4-methylphenyl)methyl]phosphonate → (5,6,7,8-Tetrahydro-3-methoxy-5,5,8,8-tetramethylnaphth-2-yl)-(4-tolyl)-acetylene

https://huagongshe.com/ja/reaction/982049

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl [chloro(4-methylphenyl)methyl]phosphonateHCID 13604830—
反応物2-Formyl-5,6,7,8-tetrahydro-3-methoxy-5,5,8,8tetramethylnaphthaleneHCID 14726522—
溶媒Dimethyl SulfoxideHCID 679—
生成物(5,6,7,8-Tetrahydro-3-methoxy-5,5,8,8-tetramethylnaphth-2-yl)-(4-tolyl)-acetyleneHCID 1360482751%

反応手順

A solution of 20.2 g (0.18 mole) of potassium tert.-butylate in 45 ml of dimethyl sulfoxide was added dropwise to a solution of 23.2 g (0.09 mole) of diethyl 1-chloro-1-(4-tolyl)-methylphosphonate and 22.1 g (0.09 mole) of 2-formyl-5,6,7,8-tetrahydro-3-methoxy-5,5,8,8-tetramethylnaphthalene in 270 ml of dry dimethyl sulfoxide at room temperature. The mixture was stirred for 30 minutes, poured onto 1 liter of ice water and extracted three times with ether. The ether phase was washed twice with water, dried over sodium sulfate and evaporated down to give 22.6 g (76%) of a slightly impure product. Recrystallization from methanol gave 15.2 g (51%) of the pure title compound of melting point 127° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04994489
出典データセットuspto-grants-1991_02
ORD IDord-9e0f159eb8da4a79b81330ddb7ecdb15
出典メモuspto-grants-1991_02