反応 #2348136

ord-12bbe2fe0da44f7ebf1496149f636703

反応方程式

CC(C)CCCC(C)CCCC(C)CCCC(C)CCO
phytanol
CC(C)CCCC(C)CCCC(C)CCCC(C)CCO
phytanol
c1ccncc1
pyridine
Cc1ccc(S(=O)(=O)Cl)cc1
p-toluenesulfonyl chloride
Cc1ccc(S(=O)(=O)OCCC(C)CCCC(C)CCCC(C)CCCC(C)C)cc1
phytanyl tosylate
収率 138.7%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他from exceeding 10° C
  2. 2
    workup.ADDITIONAfter the completion of addition, agitation
  3. 3
    その他the resulting reaction solution
  4. 4
    洗浄was successively washed with 200 ml of water, 200 ml of 2N hydrochloric acid, and 200 ml of a saturated sodium bicarbonate water
  5. 5
    乾燥dried over anhydrous magnesium sulfate
  6. 6
    ろ過After the filtration
  7. 7
    濃縮the resultant was concentrated under reduced pressure

実験手順

Under a nitrogen atmosphere, 29.16 g (97.67 mmol) of phytanol and 9.27 g (117.2 mmol) of pyridine were dissolved in 220 ml of dry methylene chloride, and 20.48 g (107.4 mmol) of p-toluenesulfonyl chloride was added little by little under ice cooling, in order to prevent the liquid temperature from exceeding 10° C. After the completion of addition, agitation was continued for 12 hours until phytanol disappeared, the resulting reaction solution was successively washed with 200 ml of water, 200 ml of 2N hydrochloric acid, and 200 ml of a saturated sodium bicarbonate water, and dried over anhydrous magnesium sulfate. After the filtration, the resultant was concentrated under reduced pressure to obtain 61.31 g of phytanyl tosylate.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07846903B2uspto-grants-2010_12