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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68210Generated: October 29, 2026

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

https://huagongshe.com/reaction/68210

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl triflateHCID 9526—
ReactantHCID 21972276HCID 21972276—
SolventDichloromethaneHCID 6344—
Product4-(Tert-butyldimethylsilyloxy)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulfonateHCID 86615371—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822233B2
Source datasetuspto-grants-2014_09
ORD IDord-c19fea5160344d28a3443bb6527dcc16
Source noteuspto-grants-2014_09