Reaktion #609977

ord-bf2d0c24b6ad4c21a5c94646a8eb0d3c

Reaktionsgleichung

CC(C)(C)OC(=O)NCCCCCCO
compound 2
CC(C)(C)OC(=O)NCCCCCCO
tert-butyl (6-hydroxyhexyl)carbamate
c1ccc(P(c2ccccc2)c2ccccc2)cc1
Ph3P
BrC(Br)(Br)Br
CBr4
CC(C)(C)OC(=O)NCCCCCCBr
compound 3
Ausbeute 78.0%
CC(C)(C)OC(=O)NCCCCCCBr
tert-butyl(6-bromohexyl)carbamate
Ausbeute 78.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with EtOAc (3×60 mL)
  2. 2
    TrocknenThe combined organic extracts were dried over Na2SO4
  3. 3
    Filtrationfiltered
  4. 4
    Einengenconcentrated in vacuo
  5. 5
    Sonstigeto obtain the crude
  6. 6
    SonstigeThe 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).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09334261B2uspto-grants-2016_05