Reaktion #1483108

ord-7720d39a9e1b424fa867ae05d833f18e

Reaktionsgleichung

CC(C)(Br)C(=O)Br
2-bromo-2-methylpropionyl bromide
CCCCCCCCCCCC(C)O
tridecan-2-ol
CCCCCCCCCCCC(C)O
2-tridecanol
CCN(CC)CC
triethylamine
C=C(CCCCCCCCCCC)OC(=O)C(C)Br
98
Ausbeute 97.6%
C=C(CCCCCCCCCCC)OC(=O)C(C)Br
tridecen-2-yl 2-bromopropanoate
Ausbeute 97.6%

Lösungsmittel

Reaktionsbedingungen

Temperatur
57.5°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction mixture was quenched with saturated sodium bicarbonate solution
  2. 2
    workup.STIRRINGstirred for 15 minutes at 25-35° C
  3. 3
    SonstigeThe aqueous and organic layers were separated
  4. 4
    WaschenThe organic layer was washed with brine
  5. 5
    Waschenthe combined organic layers were washed with brine solution
  6. 6
    TrocknenThe organic layer was dried over Na2SO4
  7. 7
    Einengenconcentrated under vacuum

Vorschrift

To a stirred solution of tridecan-2-ol 68 (5 g, 24.9 mmol) in toluene (50 mL) was added triethylamine (3.5 mL, 27.45 mmol)) and followed by 2-bromo-2-methylpropionyl bromide 97 (6.31 g, 27.45 mmol) at 5-10° C. The reaction mixture was stirred for 3 hour at 55-60° C., and the reaction was monitored by TLC. The reaction mixture was quenched with saturated sodium bicarbonate solution and stirred for 15 minutes at 25-35° C. The aqueous and organic layers were separated. The organic layer was washed with brine, and the combined organic layers were washed with brine solution. The organic layer was dried over Na2SO4 and concentrated under vacuum to afford crude 98 (8.1 g, yield: 96%) as a liquid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08900625B2uspto-grants-2014_12