Reaction #1483108

ord-7720d39a9e1b424fa867ae05d833f18e

Reaction equation

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
Yield 97.6%
C=C(CCCCCCCCCCC)OC(=O)C(C)Br
tridecen-2-yl 2-bromopropanoate
Yield 97.6%

Solvents

Conditions

Temperature
57.5°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

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

Procedure

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.

Source

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