반응 #48689

ord-6975154842644f7fbddb9e327f2bcaee

반응 방정식

O=S(=O)(OS(=O)(=O)C(F)(F)F)C(F)(F)F
trifluoromethanesulphonic anhydride
CC(C)(C)CO
neopentylalcohol
Cc1cccc(C)n1
2,6-lutidine
CC(C)(C)COS(=O)(=O)C(F)(F)F
desired compound
수율 72.0%
CC(C)(C)COS(=O)(=O)C(F)(F)F
Trifluoromethanesulfonic acid 2,2-dimethylpropyl ester
수율 72.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Add water to quench
  2. 2
    기타the reaction
  3. 3
    기타separate the organic layer
  4. 4
    추출extract the aqueous layer with dichloromethane
  5. 5
    건조dry (magnesium sulfate)
  6. 6
    여과filter
  7. 7
    농축concentrate
  8. 8
    기타purify
  9. 9
    세척(silica gel chromatography, eluting with 1:4 hexane:dichloromethane)

실험 절차

Add trifluoromethanesulphonic anhydride (1.12 mL, 6.8 mmol) to a solution of neopentylalcohol (0.5 g, 5.7 mmol) and 2,6-lutidine (0.7 mL, 6.8 mmol) in dichloromethane (10 mL) at −78° C. and stir for 1 hour. Add water to quench the reaction, separate the organic layer and extract the aqueous layer with dichloromethane. Combine the organic layers, dry (magnesium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 1:4 hexane:dichloromethane) to give the desired compound as an oil (0.9 g, 72% yield).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07745438B2uspto-grants-2010_06