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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1614249Erstellt: 25. Oktober 2026

Hydrochloric Acid → HCID 19773292, Verbindung

https://huagongshe.com/reaction/1614249

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt2-Thiopheneethylamine, hydrochlorideHCID 458572—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt5-Acetylamino-2-tetraloneHCID 14836456—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
ProduktHCID 19773292HCID 19773292—

Reaktionsschritte

2.03 g of (0.01 mol) of 5-acetylamino-2-tetralone, 3.2 g (0.02 mol) of 2-(2-thienyl)-ethyl-aminehydrochloride and 0.75 g (0.012 mol) of sodium cyanoborohydride are dissolved in 30 ml of methanol and stirred for 24 hours at ambient temperature. The mixture is then acidified by the dropwise addition of conc. hydrochloric acid with stirring and cooling with ice. After 10 minutes, 100 ml of water is added whilst stirring continues and then a total of 4.0 g of anhydrous soda is added in batches. Then extraction is carried out with 50 ml of methylene chloride and twice with 25 ml of methylene chloride. The combined extracts are washed with 20 ml of water, dried with sodium sulphate and after separation of the drying agent, concentrated by evaporation in a rotary evaporator, finally at 90° C. and under a complete water-jet vacuum. The residue is dissolved with 5 ml of methanol and 4.0 ml of 2.5 N ethanolic hydrochloric acid and the solution is mixed with diethylether until turbidity is just beginning. After standing for a period of about 12 hours at 5° C. the title compound is suction filtered, washed with ethanol/ether and dried at 80° C. until the weight remains constant. Yield: 3.1 g (88.3% of theory), melting point 276° C. (unchanged after recrystallisation from methanol/ether).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05196454
Quelldatensatzuspto-grants-1993_03
ORD IDord-d5a8b3f7b2c645b698bc401246eb4743
Quellennotizuspto-grants-1993_03