反応 #1914826

ord-bcc0d53ee57a42dc907058638372cacf

反応方程式

OCCCCCCCCCCCCCCCCBr
16-bromohexadecan-1-ol
Cl
HCl
[Na]
sodium
[Na+].[OH-]
NaOH
O=C(O)Cc1cccs1
thiolacetic acid
OCCCCCCCCCCCCCCCCS
desired product
収率 70.3%
OCCCCCCCCCCCCCCCCS
16-Mercaptohexadecan-1-ol
収率 70.3%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONAfter completion of addition the reaction mixture
  2. 2
    workup.STIRRINGAfter additional 10 min of stirring 3 ml
  3. 3
    workup.ADDITIONwere added
  4. 4
    温度The resulted mixture was refluxed for 15 hrs
  5. 5
    温度to cool to RT
  6. 6
    温度The reaction completion required additional 3 hr of reflux
  7. 7
    その他Resulted
  8. 8
    その他reaction mixture
  9. 9
    温度was cooled with ice bath
  10. 10
    workup.ADDITIONpoured
  11. 11
    workup.STIRRINGwith stirring, into a vessel
  12. 12
    抽出extracted with 300 ml of ether
  13. 13
    その他The organic layer was separated
  14. 14
    洗浄washed with 3×150 ml of water, 150 ml of saturated NaCl aqueous solution
  15. 15
    乾燥dried over sodium sulfate
  16. 16
    その他After ether removal material
  17. 17
    workup.DISSOLUTIONwas dissolved in minimum amount of dicloromethane
  18. 18
    その他purified by silica gel chromatography (100% dicloromethane as eluent)

実験手順

Under inert atmosphere 365 mg of sodium metal suspension (40% in mineral oil) were added dropwise to 20 ml of dry methanol at 0° C. After completion of addition the reaction mixture was stirred for 10 min at RT followed by addition of 0.45 ml (6.30 mmole) of thiolacetic acid. After additional 10 min of stirring 3 ml degassed methanolic solution of 1.0 gr (3.11 mmole) of 16-bromohexadecan-1-ol were added. The resulted mixture was refluxed for 15 hrs, allowed to cool to RT and 20 ml of degassed 1.0 M NaOH aqueous solution were injected. The reaction completion required additional 3 hr of reflux. 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 ether removal material was dissolved in minimum amount of dicloromethane and purified by silica gel chromatography (100% dicloromethane as eluent). 600 mg (70% yield) of the desired product were obtained.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07056669B2uspto-grants-2006_06