Reaktion #88162

Reaktionsgleichung

2-ethoxyphenol

tert-butyl (S)-3-hydroxypiperidine-1-carboxylate

triphenylphosphine

DIAD

→

tert-butyl (R)-3-(2-ethoxyphenoxy)piperidine-1-carboxylate

Ausbeute 45.9%

Lösungsmittel

toluene

toluene

Reaktionsbedingungen

Aufarbeitung

1. 1
   Filtrationthe reaction mixture was filtered
2. 2
   Waschenwashed with diethyl ether (300 mL)
3. 3
   WaschenThe filtrate was washed with 3N NaOH (150 mL)
4. 4
   Trocknendried over Na2SO4
5. 5
   Einengenconcentrated
6. 6
   SonstigeThe crude residue was purified via column chromatography

Vorschrift

To a solution of 2-ethoxyphenol (13.72 g, 99 mmol), tert-butyl (S)-3-hydroxypiperidine-1-carboxylate (20 g, 99 mmol), and triphenylphosphine (29 g, 111 mmol) in toluene (150 mL) at 20-25° C. was added a solution of DIAD (20 mL, 104 mmol) in toluene (50 mL) over 2 hours. After 2 hours, the reaction mixture was filtered and washed with diethyl ether (300 mL). The filtrate was washed with 3N NaOH (150 mL), dried over Na2SO4, and concentrated. The crude residue was purified via column chromatography to afford tert-butyl (R)-3-(2-ethoxyphenoxy)piperidine-1-carboxylate (14.6 g, 45%). MS (ES+) 222.2 (M-100+H).

Quelle