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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1243047Erstellt: 25. Oktober 2026

Isopropanol → trans-2-(2-Chlorophenylamino)cyclohexanol

https://huagongshe.com/reaction/1243047

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsopropanolHCID 3776—
Edukt1-Chloro-2-iodobenzeneHCID 11993—
EduktSodium HydroxideHCID 14798—
Edukt2-Aminocyclohexanol hydrochlorideHCID 21877202—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkttrans-2-(2-Chlorophenylamino)cyclohexanolHCID 1171556591%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A 15 mL screw top test tube fitted with a PTFE septum cap was purged with argon before addition of CuI (5.0 mg, 0.026 mmol, 2.6 mol %), NaOH (125 mg, 3.12 mmol) and rac-2-amino-1-cyclohexanol HCl (158 mg, 1.04 mmol). 2-Chloro-1-iodobenzene (152 μL, 1.25 mmol) and isopropyl alcohol (1.0 mL) were added, via syringe, under argon. The septum cap was replaced with a solid, Teflon-lined cap and the reaction was stirred magnetically at 90° C. for 48 h. The resulting homogeneous solution was allowed to cool before dilution with 10 mL brine. The reaction mixture was transferred to a separatory funnel and extracted with methylene chloride (3×10 mL). The organics were washed with brine, dried over MgSO4 and concentrated. The crude material was purified by silica gel chromatography using hexanes/ethyl acetate (60:40). The product was obtained as a yellow oil in 91% yield (212.7 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07115784B2
Quelldatensatzuspto-grants-2006_10
ORD IDord-5904c8bb0fb74a948fc75f0e7e0db299
Quellennotizuspto-grants-2006_10