Methyl triflate → 4-(Tert-butyldimethylsilyloxy)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulfonate

HRID 1425643Notes

Reaction equation

HRID 1425643 reaction equation
[CH:1]1[C:14]2[C:5](=[N:6][C:7]3[C:12]([C:13]=2[C:15]([O:17][C:18]2[CH:23]=[CH:22][C:21]([O:24][Si:25]([C:28]([CH3:31])([CH3:30])[CH3:29])([CH3:27])[CH3:26])=[CH:20][CH:19]=2)=[O:16])=[CH:11][CH:10]=[CH:9][CH:8]=3)[CH:4]=[CH:3][CH:2]=1.[F:32][C:33]([F:40])([F:39])[S:34]([O:37]C)(=[O:36])=[O:35]>ClCCl>[F:32][C:33]([F:40])([F:39])[S:34]([O-:37])(=[O:36])=[O:35].[CH3:33][N+:6]1[C:7]2[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=2)[C:13]([C:15]([O:17][C:18]2[CH:19]=[CH:20][C:21]([O:24][Si:25]([C:28]([CH3:31])([CH3:30])[CH3:29])([CH3:26])[CH3:27])=[CH:22][CH:23]=2)=[O:16])=[C:14]2[C:5]=1[CH:4]=[CH:3][CH:2]=[CH:1]2

Participants

4

Procedure

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.

Workup

  1. customInto a 50 mL round bottom flask equipped with magnetic stirrer under argon atmosphere
  2. filtrationBright yellow solid was collected by filtration
  3. washwashed with 2×1 mL of dichloromethane and air
  4. customdried for 4 hr

Sources & evidence

ORD record
ord-7bfc73ad9ec540998a54c47b656466e0
Source dataset
uspto-grants-2015_01
Patent number
US08932881B2

Reaction notes

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