Reaction #833542

ord-7d0e5610022d4caa842357aab5998499

Reaction equation

O=C(O)CCCCCCCCCCCCCCCBr
16bromohexadecanoic acid
Cl
HCl
[Na]
sodium
[Na+].[OH-]
NaOH
CC(O)=S
thioacetic acid
O=C(O)CCCCCCCCCCCCCCCS
desired product
Yield 97.2%
O=C(O)CCCCCCCCCCCCCCCS
16-Mercaptohexadecanoic acid
Yield 97.2%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.ADDITIONAt the end of the addition reaction mixture
  2. 2
    workup.STIRRINGAfter additional 10 min of stirring
  3. 3
    workup.ADDITIONwere added
  4. 4
    TemperatureThe resulted mixture was refluxed for 15 hrs
  5. 5
    Temperatureto cool to RT
  6. 6
    TemperatureAdditional refluxing for 3 hrs
  7. 7
    Otherrequired for reaction completion
  8. 8
    OtherResulted
  9. 9
    Otherreaction mixture
  10. 10
    Temperaturewas cooled with ice bath
  11. 11
    workup.ADDITIONpoured
  12. 12
    workup.STIRRINGwith stirring, into a vessel
  13. 13
    Extractionextracted with 300 ml of ether
  14. 14
    OtherThe organic layer was separated
  15. 15
    Washwashed with 3×150 ml of water, 150 ml of saturated NaCI aqueous solution
  16. 16
    Dryingdried over sodium sulfate
  17. 17
    OtherAfter removal of ether material
  18. 18
    Otherwas purified by recrystallization from n-hexane
  19. 19
    Filtrationfiltering out
  20. 20
    Otherdrying over high vacuum

Procedure

Under inert atmosphere 2.0 gr of sodium metal suspension (40% in mineral oil) were slowly added to 100 ml of dry methanol at 0° C. At the end of the addition reaction mixture was stirred for 10 min at RT and 1.75 ml (21.58 mmole) of thioacetic acid were added. After additional 10 min of stirring, 30 ml degassed methanolic solution of 6.1 gr (18.19 mmole) of 16bromohexadecanoic acid were added. The resulted mixture was refluxed for 15 hrs, after which, allowed to cool to RT and 50 ml of degassed 1.0 M NaOH aqueous solution were injected. Additional refluxing for 3 hrs required for reaction completion. Resulted reaction mixture was cooled with ice bath and poured, with stirring, into a vessel containing 200 ml of ice water. This mixture was titrated to pH=7 by 1.0 M HCl and extracted with 300 ml of ether. The organic layer was separated, washed with 3×150 ml of water, 150 ml of saturated NaCI aqueous solution and dried over sodium sulfate. After removal of ether material was purified by recrystallization from n-hexane, filtering out and drying over high vacuum. 5.1 gr (97% yield) of the desired product was obtained.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07393645B2uspto-grants-2008_07