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HRID 22134作成日:2026年10月26日

Ammonium Hydroxide → 2-Di-n-propylamino-8-(fur-3-yl)-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/22134

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium HydroxideHCID 14923—
反応物3-BromofuranHCID 89164—
反応物MagnesiumHCID 5462224—
反応物8-Bromo-2-dipropylamino-1,2,3,4-tetrahydronaphthaleneHCID 14529564—
触媒1,1-DibromoethaneHCID 11201—
触媒HCID 178418751HCID 178418751—
触媒HCID 178420538HCID 178420538—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
生成物2-Di-n-propylamino-8-(fur-3-yl)-1,2,3,4-tetrahydronaphthaleneHCID 1522242984.1%

反応条件

温度0 °C

反応手順

2-Di-n-propylamino-8-bromo-1,2,3,4-tetrahydronaphthalene (1.0 g; 3.2 mmol) was dissolved in 20 ml of THF, and 94 mg (3.9 mmol) of magnesium shavings were added. The mixture was refluxed, and a couple of drops of dibromoethane were added to initiate Grignard formation. The mixture was refluxed for one hour after which it was added to a solution of 0.58 ml (6.4 mmol) of 3-bromofuran and 36 mg (0.03 mmol) of Ni(PPh3)4 in 20 ml of toluene that had been cooled to 0° C. after stirring at room temperature for one hour. The mixture was stirred at room temperature for three hours after which an additional 0.58 ml of 3-bromofuran and 35 mg of Ni(PPh3)4 were added. When the reaction failed to proceed further, 210 mg (0.3 mmol) Ni(PPh3)2Cl2 was added, and the mixture was stirred overnight at room temperature. The mixture then was poured into water and the pH adjusted to 10 with ammonium hydroxide. The mixture was extracted with methylene chloride, dried over sodium sulfate, and evaporated to give 0.8 g of a residue.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05426226
出典データセットuspto-grants-1995_06
ORD IDord-d34262a676634d269babbf51150d3970
出典メモuspto-grants-1995_06