تفاعل #1914824

ord-67e324bef92c4519b742d158c0daf6f2

معادلة التفاعل

O=C(O)CCCCCCCCCCCCCCCBr
16-bromohexadecanoic acid
Cl
HCl
[Na]
sodium
[Na+].[OH-]
NaOH
O=C(O)Cc1cccs1
thiolacetic acid
O=C(O)CCCCCCCCCCCCCCCS
desired product
المردود 97.2%
O=C(O)CCCCCCCCCCCCCCCS
16-Mercaptohexadecanoic acid
المردود 97.2%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  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
    درجة الحرارةThe resulted mixture was refluxed for 15 hrs
  5. 5
    درجة الحرارةto cool to RT
  6. 6
    درجة الحرارةAdditional refluxing for 3 hrs
  7. 7
    أخرىrequired for reaction completion
  8. 8
    أخرىResulted
  9. 9
    أخرىreaction mixture
  10. 10
    درجة الحرارةwas cooled with ice bath
  11. 11
    workup.ADDITIONpoured
  12. 12
    workup.STIRRINGwith stirring, into a vessel
  13. 13
    استخلاصextracted with 300 ml of ether
  14. 14
    أخرىThe organic layer was separated
  15. 15
    غسيلwashed with 3×150 ml of water, 150 ml of saturated NaCl aqueous solution
  16. 16
    تجفيفdried over sodium sulfate
  17. 17
    أخرىAfter removal of ether material
  18. 18
    أخرىwas purified by recrystalization from n-hexane
  19. 19
    ترشيحfiltering out
  20. 20
    أخرىdrying over high vacuum

الإجراء التجريبي

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 thiolacetic acid were added. After additional 10 min of stirring, 30 ml degassed methanolic solution of 6.1 gr (18.19 mmole) of 16-bromohexadecanoic 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 NaCl aqueous solution and dried over sodium sulfate. After removal of ether material was purified by recrystalization from n-hexane, filtering out and drying over high vacuum. 5.1 gr (97% yield) of the desired product were obtained.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07056669B2uspto-grants-2006_06