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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9331Erstellt: 24. Oktober 2026

Benzyloxyamine hydrochloride → HCID 178419047, Verbindung

https://huagongshe.com/de/reaction/9331

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyloxyamine hydrochlorideHCID 102312—
Edukt5'-Bromo-2'-(methylthio)spiro[cyclohexane-1,3'-[3H]indole]HCID 21986266—
LösungsmittelMethanolHCID 887—
ProduktHCID 178419047HCID 178419047—

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

5′-Bromo-2′-(methylthio)spiro[cyclohexane-1,3′-[3H]indole] (9.0 g, 28.98 mmol) and O-benzylhydroxylamine hydrochloride (13.8 g, 86.9 mmol) were combined in methanol (150 mL) and heated to 45° C. for 6 hours. Methanol was evaporated in vacuo. Ethyl acetate was added to the residue and this mixture was washed with ammonium chloride solution. Ethyl acetate was dried over magnesium sulfate, ethyl acetate collected evaporated in vacuo and the residue was flash chromatographed on alumina 90 (9:1 Hexane/EtOAc) to the desired product (6.5 g, 60%). 1H NMR (DMSO-d6, 300 MHz) δ 1.38–1.70 (m, 8H), 1.92–2.06 (m, 2H), 5.06 (s, 2H), 6.71 (d, 1H, J=8.26 Hz), 7.22–7.43 (m, 7H), 9.62 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091234B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-2a5db7c4f64e47bcb8b812a4d9f7db0b
Quellennotizuspto-grants-2006_08