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52704-48-0

2-(3,4-Dihydroquinolin-1(2H)-yl)ethanol synthesis

9synthesis methods
-

Yield:52704-48-0 45% ,5840-01-7 45%

Reaction Conditions:

with palladium on activated charcoal;zinc(II) oxide in water at 150; for 24 h;Sealed tube;

Steps:

4.1. General procedure

General procedure: 1 mmol of amine, 0.07 mmol of Pd/C, 3 mmol of ZnO, 6 mL of distilled water and 6 mL of ethylene glycol were mixed manually inside a 20 mL Teflon flask. Then it was sealed into a steel autoclave and introduced in a preheated oven at 150 °C for 24 h. The reaction mixture was cooled to room temperature, 25 mL of distilled water were added and the crude was filtered through a 0.2 mm Teflon filter. The reaction mixture was extracted with ethyl acetate3 15 ml and organic layers were combined, dried with Na2SO4, filtered and concentrated affording the reaction crude that was cheeked by NMR. Crude reaction was purified by chromatotron (1 mm, silica, from hexane to hexane/AcOEt 1:3) affording pure β-amino alcohols.

References:

Llabres-Campaner, Pedro J.;Ballesteros-Garrido, Rafael;Ballesteros, Rafael;Abarca, Belén [Tetrahedron,2017,vol. 73,# 37,p. 5552 - 5561] Location in patent:supporting information