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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 63582Erstellt: 23. Oktober 2026

Acetic Acid → 2-[(1H-Indol-7-ylmethyl)amino]-ethan-1-ol

https://huagongshe.com/de/reaction/63582

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktAcetaldehyde ammoniaHCID 522583—
EduktIndole-7-carboxaldehydeHCID 2734629—
EduktSodium triacetoxyborohydrideHCID 5049666—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt2-[(1H-Indol-7-ylmethyl)amino]-ethan-1-olHCID 21950050—

Reaktionsschritte

To a solution of 7-formyl indole (2.4 g, 16.6 mmol) in 1,2-dichloroethane (60 mL) was added aminoethanol (1.2 mL, 19.8 mmol) followed by glacial acetic acid (2.0 mL) and sodium triacetoxyborohydride (3.5 g, 16.6 mmol). The reaction mixture was allowed to stir at room temperature for 16 hours. The reaction mixture was quenched by addition of water (10 mL) and 1.0 M sodium hydroxide (10 mL). The organic layer was then separated and the aqueous layer extracted with 1,2-dichloroethane (40 mL). The combined organic extracts were washed with saturated sodium bicarbonate (2×30 mL), water (2×50 mL), dried over anhydrous sodium sulfate and evaporated to dryness. 2-[(1H-indol-7-ylmethyl)-amino]-ethanol (4.4 g) was obtained as an oil LCMS (M+H)=189.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447088B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-6d082143eacc4623b3cf5fbe2eb69011
Quellennotizuspto-grants-2016_09