반응 #155392

ord-c19fea5160344d28a3443bb6527dcc16

반응 방정식

CC(C)(C)[Si](C)(C)Oc1ccc(OC(=O)c2c3ccccc3nc3ccccc23)cc1
4-(tert-butyldimethylsilyloxy)phenyl acridin-9-carboxylate
COS(=O)(=O)C(F)(F)F
methyl trifluoromethanesulfonate
C[n+]1c2ccccc2c(C(=O)Oc2ccc(O[Si](C)(C)C(C)(C)C)cc2)c2ccccc21.O=S(=O)([O-])C(F)(F)F
4-(tert-butyldimethylsilyloxy)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulfonate

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Into a 50 mL round bottom flask equipped with magnetic stirrer under argon atmosphere
  2. 2
    여과Bright yellow solid was collected by filtration
  3. 3
    세척washed with 2×1 mL of dichloromethane and air
  4. 4
    기타dried for 4 hr

실험 절차

Into a 50 mL round bottom flask equipped with magnetic stirrer under argon atmosphere charged a solution of 1.6 parts of 4-(tert-butyldimethylsilyloxy)phenyl acridin-9-carboxylate in 25 mL of dichloromethane. 3.2 Parts of methyl trifluoromethanesulfonate was added to the solution and stirred for 40 hrs at room temperature. Bright yellow solid was collected by filtration, washed with 2×1 mL of dichloromethane and air dried for 4 hr to yield 1.44 parts of 4-(tert-butyldimethylsilyloxy)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulfonate having the following structure confirmed by NMR.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08822233B2uspto-grants-2014_09