反応 #1951043

ord-578b490032b5403087cde397d307b7d0

反応方程式

Cc1ccc(S(=O)(=O)Cl)cc1
tosyl chloride
CC(C)C=CO
isopentenol
CCCCCC
hexane
C=C(C)CCOS(=O)(=O)c1ccc(C)cc1
3-methyl-3-butene-1-yl tosylate
収率 85.3%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他is equipped
  2. 2
    その他has been carefully dried
  3. 3
    workup.ADDITIONare slowly added to this mixture through a septum
  4. 4
    その他resulting in the immediate formation of a white precipitate
  5. 5
    ろ過The mixture is then filtered
  6. 6
    濃縮the filtrate concentrated by evaporation under reduced pressure
  7. 7
    workup.ADDITIONThe solution is then diluted with diethyl ether
  8. 8
    その他Once the solvent has evaporated
  9. 9
    その他a yellowish oil is obtained
  10. 10
    その他The product is purified by preparative chromatography through a silica column (silica gel 60; eluent: pentane/ethyl acetate 85/15)

実験手順

2.32 mmol (442 mg) of tosyl chloride and 2.55 mmol (312 mg) of 4-(N,N-dimethylamino)pyridine are introduced while stirring with a magnetic stirrer into 5 ml of anhydrous dichloromethane in a glass reaction vessel which is equipped for handling under an inert atmosphere and has been carefully dried. 2.32 mmol (200 mg) of isopentenol dissolved in approx. 1 ml of dichloromethane are slowly added to this mixture through a septum using a syringe. The reaction is monitored by thin-layer chromatography on silica (silica gel 60 F-254; eluent: pentane/ethyl acetate 85/15 vol./vol.; Rf (product)=0.4 and Rf (TsCl)=0.5). After approx. 3 hours' stirring under a nitrogen atmosphere, the reaction mixture is diluted in a large volume of hexane (approx. 100 ml), resulting in the immediate formation of a white precipitate. The mixture is then filtered and the filtrate concentrated by evaporation under reduced pressure. The solution is then diluted with diethyl ether and refiltered. Once the solvent has evaporated, a yellowish oil is obtained. The product is purified by preparative chromatography through a silica column (silica gel 60; eluent: pentane/ethyl acetate 85/15). In this manner, 1.98 mmol (475 mg) of 3-methyl-3-butene-1-yl tosylate (85% isolated yield) are obtained. The compound (colorless oil) is stored at +4° C. in an anhydrous medium.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07625879B2uspto-grants-2009_12