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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1179060Erstellt: 27. Oktober 2026

1,2-Dichloroethane → N'-Benzo[b]thiophen-5-yl-N,N-dimethyl-1-phenyl-cyclohexane-1,4-diamine hydrochloride

https://huagongshe.com/reaction/1179060

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
EduktAcetic AcidHCID 176—
EduktBenzo(b)thiophen-5-amineHCID 288032—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt4-(Dimethylamino)-4-phenylcyclohexan-1-oneHCID 11424492—
ProduktN'-Benzo[b]thiophen-5-yl-N,N-dimethyl-1-phenyl-cyclohexane-1,4-diamine hydrochlorideHCID 69337854—
ProduktN'-benzo[b]thiophen-5-yl-N,N-dimethyl-1-phenyl-cyclohexane-1,4-diamineHCID 69337855—

Reaktionsschritte

300 mg 5-Aminobenzothiophene and 435 mg 4-dimethylamino-4-phenyl-cyclohexanone were dissolved in dry 1,2-dichloroethane (20 ml) under argon. Glacial acetic acid (2 mmol) and 600 mg sodium triacetoxyborohydride were added to this mixture and the mixture was stirred for 24 hours at RT. For working up, the reaction mixture was concentrated and the residue was adjusted to pH 11 with five molar sodium hydroxide solution. The alkaline phase was diluted with water (10 ml) and extracted with ethyl acetate (3×20 ml). The combined extracts were dried over sodium sulfate and filtered and the filtrate was concentrated. The crude product was chromatographed over silica gel with ethyl acetate/ethanol (1:1). 230 mg of the nonpolar diastereomer of N′-benzo[b]thiophen-5-yl-N,N-dimethyl-1-phenyl-cyclohexane-1,4-diamine were obtained as a white solid, from which the corresponding hydrochloride was precipitated with 1.85 M ethanolic hydrochloric acid (0.54 ml) in 2-butanone (8 ml) (243 mg; m.p. 155-157° C.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07276518B2
Quelldatensatzuspto-grants-2007_10
ORD IDord-bc78de4c9cb84a019a9fe4c0ef171897
Quellennotizuspto-grants-2007_10