Hydrogen Bromide → 1,2,3,4-Tetrahydroisoquinolin-8-ol

Reaktionsgleichung

C[O:2][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:12]=1[CH2:11][NH:10][CH2:9][CH2:8]2.Br>>[CH2:11]1[C:12]2[C:7](=[CH:6][CH:5]=[CH:4][C:3]=2[OH:2])[CH2:8][CH2:9][NH:10]1

Komponenten

Edukt 2

HCID 260Hydrogen Bromide

HCID 129507478-Methoxy-1,2,3,4-tetrahydroisoquinoline

Produkt 1

HCID 136352141,2,3,4-Tetrahydroisoquinolin-8-olAusbeute 80,4 %

Versuchsvorschrift

Combine 8-Methoxy-tetrahydroisoquinoline (665.7 mg, 4.08 mmol) and 48% HBr at room temperature. Reflux the reaction for 3 hours and then cool to room temperature. Recrystallize the product from EtOH and Diethyl ether to afford 754.2 mg, 3.28 mmol (80% yield) of the title compound as a tannish white solid: 1H NMR (500 MHz, DMSO); 2.9 (2H, t, J=6.16, 5.86), 3.2-3.4 (2H, m), 4.0 (2H, s), 6.6-6.8 (2H, m), 7.0-7.1 (1H, m), 8.8-9.1 (2H, b m), 9.9 (1H, s); MS m/z 148 (M+).

Aufarbeitung

customat room temperature
temperatureReflux
customthe reaction for 3 hours
customRecrystallize the product from EtOH and Diethyl ether

Quellen und Nachweise

ORD-Eintrag: ord-296d7719518240b89179e7b37abb4b4e
Quelldatensatz: uspto-grants-2008_06
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US07381719B2

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