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HRID 428222作成日:2026年10月26日

1,1-Dibromoethane → 3-(5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-1-propyne

https://huagongshe.com/reaction/428222

反応式

関与物質

役割名称HCID仕込み量
反応物1,1-DibromoethaneHCID 11201—
反応物Ammonium ChlorideHCID 25517—
反応物1-Methoxypropa-1,2-dieneHCID 139403—
反応物6-Bromo-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthaleneHCID 226685—
反応物MagnesiumHCID 5462224—
溶媒TetrahydrofuranHCID 8028—
生成物3-(5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-1-propyneHCID 1777386947%

反応条件

温度50 °C

反応手順

20 g (0.82 mol) of magnesium activated with 0.1 ml of dibromoethane are introduced into a four litre reactor under a stream of nitrogen. A solution of 200 g (0.75 mol) of 2-bromo-5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphthalene is added dropwise so as to maintain the reflux of the THF and the mixture is stirred at 50° C. for two hours. The reaction medium is then cooled to −5° C. and 1.2 g (8.2 mmol) of CuBr are added and a solution of 58 g (0.82 mol) of methoxyallene in 100 ml of THF is introduced dropwise. The mixture is stirred for one hour at −5° C. and is then allowed to return to room temperature and is stirred for two hours. The reaction medium is poured into saturated ammonium chloride solution and extracted with ethyl acetate, and the organic phase is separated out after settling has taken place, dried over magnesium sulphate and evaporated. The oil obtained is distilled at 0.02 mm Hg and the fraction passing at 95-100° C. is collected. 79 g (47%) of the expected product are obtained in the form of a colourless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313162B1
出典データセットuspto-grants-2001_11
ORD IDord-6c3aed9c74eb4c98968b6f85f068140e
出典メモuspto-grants-2001_11