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HRID 22134Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/22134

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium HydroxideHCID 14923—
Edukt3-BromofuranHCID 89164—
EduktMagnesiumHCID 5462224—
Edukt8-Bromo-2-dipropylamino-1,2,3,4-tetrahydronaphthaleneHCID 14529564—
Katalysator1,1-DibromoethaneHCID 11201—
KatalysatorHCID 178418751HCID 178418751—
KatalysatorHCID 178420538HCID 178420538—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Di-n-propylamino-8-(fur-3-yl)-1,2,3,4-tetrahydronaphthaleneHCID 1522242984,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05426226
Quelldatensatzuspto-grants-1995_06
ORD IDord-d34262a676634d269babbf51150d3970
Quellennotizuspto-grants-1995_06