Reaktion #1483102

ord-6983ec8315074454a9cd88da83c107a6

Reaktionsgleichung

CC(Br)C(=O)Br
2-bromo propionyl bromide
CCCCCCCCCCCCO
1-decanol
CCCCCCCCCCCCO
1-dodecanol
CCN(CC)CC
triethylamine
CCCCCCCCCCCCOC(=O)C(C)Br
59
Ausbeute 94.0%
CCCCCCCCCCCCOC(=O)C(C)Br
dodecyl 2-bromopropanoate
Ausbeute 94.0%

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 1-decanol 2 (10 g, 53.7 mmol) in toluene (100 mL) was added triethylamine (7.5 mL, 53.7 mmol)) and followed by 2-bromo propionyl bromide 58 (12.7 g, 59.1 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 59 (16.2 g, yield: 94%) as a liquid.

Quelle

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