反応 #1121768

ord-b6810416db3547f3b5176b2ef8b9bf9e

反応方程式

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

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他Into a 50 mL round bottom flask equipped with magnetic stirrer under argon atmosphere
  2. 2
    ろ過Bright yellow solid was collected by filtration
  3. 3
    洗浄washed with 2×1 mL of dichloromethane and air
  4. 4
    その他dried for 4 hr

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08546150B2uspto-grants-2013_10