Reaktion #569264

Reaktionsgleichung

2-Chlorobenzenesulfonic acid 3 -[[N-(tert-butoxycarbonyl)piperidin-4-yl]-methoxy]phenyl ester

HCl

→

title compound

Ausbeute 79.0%

2-Chlorobenzenesulfonic acid 3-[(piperidin-4-yl)methoxy]phenyl ester

Ausbeute 79.0%

Lösungsmittel

1,4-dioxan

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeAfter removing the solvent in vacuo
2. 2
   Sonstigethe residue was purified by flash column chromatography (5% methanol in methylene chloride to 5% methanol in methylene chloride saturated with NH3)

Vorschrift

2-Chlorobenzenesulfonic acid 3 -[[N-(tert-butoxycarbonyl)piperidin-4-yl]-methoxy]phenyl ester (565 mg, 1.2 mmol), as prepared in the preceding step, was treated with 30 mL of 4N HCl in 1,4-dioxan and stirred at room temperature for 2 h. After removing the solvent in vacuo, the residue was purified by flash column chromatography (5% methanol in methylene chloride to 5% methanol in methylene chloride saturated with NH3) to give the title compound as a white foam (360 mg, 79%). 1H-NMR (300 MHz, CDCl3) δ 1.50 (m, 2H), 1.91 (m, 3H), 2.77 (t, 2H), 3.33 (d, 2H), 3.73 (d, 2H), 4.44 (bs, 1H), 6.69 (m, 2H), 6.77 (dd, 1H), 7.16 (t, 1H), 7.37 (t, 1H), 7.62 (m, 2H), 7.95 (dd, 1H). Mass spectrum (MALDI-TOF, sinapinic acid matrix) calcd. for C18H20NO4SCl: 382.1 (M+H), 404.1 (M+Na). Found: 382.1, 404.5.

Quelle