反应 #833544

ord-a2571d6524564545adc7cb047ffe1c88

反应方程式

OCCCCCCCCCCCCCCCCBr
16-bromohexadecan-l-ol
Cl
HCl
[Na]
sodium
[Na+].[OH-]
NaOH
CC(O)=S
thioacetic acid
OCCCCCCCCCCCCCCCCS
desired product
收率 70.3%
OCCCCCCCCCCCCCCCCS
16-Mercaptohexadecan-l-ol
收率 70.3%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  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
    其他Resulted
  8. 8
    其他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
    萃取extracted with 300 ml of ether
  13. 13
    其他The organic layer was separated
  14. 14
    洗涤washed with 3×150 ml of water, 150 ml of saturated NaCl aqueous solution
  15. 15
    干燥dried over sodium sulfate
  16. 16
    其他After ether removal material
  17. 17
    workup.DISSOLUTIONwas dissolved in minimum amount of dichloromethane
  18. 18
    其他purified by silica gel chromatography (100% dichloromethane as eluent)

实验过程

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 thioacetic acid. After additional 10 min of stirring 3 ml degassed methanolic solution of 1.0 gr (3.11 mmole) of 16-bromohexadecan-l-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 dichloromethane and purified by silica gel chromatography (100% dichloromethane as eluent). 600 mg (70% yield) of the desired product were obtained.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07393645B2uspto-grants-2008_07