Reaktion #609977
ord-bf2d0c24b6ad4c21a5c94646a8eb0d3c
Reaktionsgleichung
compound 2
tert-butyl (6-hydroxyhexyl)carbamate
Ph3P
CBr4
→
compound 3
Ausbeute 78.0%
tert-butyl(6-bromohexyl)carbamate
Ausbeute 78.0%
Reagenzien
Keine
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Extraktionextracted with EtOAc (3×60 mL)
- 2TrocknenThe combined organic extracts were dried over Na2SO4
- 3Filtrationfiltered
- 4Einengenconcentrated in vacuo
- 5Sonstigeto obtain the crude
- 6SonstigeThe crude was purified (silica gel; 20% EtOAc/hexanes)
Vorschrift
To a stirred solution of compound 2 (1 g, 4.61 mmol) in toluene (30 mL) were added Ph3P (1.81 g, 6.91 mmol) and CBr4 (2.29 g, 6.91 mmol) at RT under inert atmosphere and stirred for 3 h. The mixture was diluted with water (50 mL) and extracted with EtOAc (3×60 mL). The combined organic extracts were dried over Na2SO4, filtered and concentrated in vacuo to obtain the crude. The crude was purified (silica gel; 20% EtOAc/hexanes) to afford compound 3 (1 g, 78%) as colorless oil. 1H NMR (400 MHz, CDCl3): δ 4.51 (br s, 1H), 3.40 (t, J=6.8 Hz, 2H), 3.13-3.08 (m, 2H), 1.89-1.82 (m, 2H), 1.52-1.42 (m, 13H), 1.37-1.31 (m, 2H).