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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901793Generated: October 30, 2026

Trifluoromethanesulfonic acid → HCID 67157467, compound

https://huagongshe.com/reaction/901793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantBenzyl 2,2,2-trichloroacetimidateHCID 144968—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67157509HCID 67157509—
SolventEthyl AcetateHCID 8857—
SolventDichloromethane cyclohexaneHCID 21916607—
ProductHCID 67157467HCID 6715746772%

Reaction Steps

The compound (344 mg, 0.92 mmol) synthesized in Example 10 (10a) was dissolved in methylene chloride:cyclohexane (1:2, 10 mL) and benzyl trichloroacetoimidate (0.68 mL, 3.68 mmol) and trifluoromethane sulfonic acid (16 μL, 0.18 mmol) were added thereto, followed by stirring of the mixture at room temperature for 4 hours. After saturated aqueous sodium hydrogencarbonate (1 mL) was added to the reaction mixture at 0° C. and the mixture was diluted with ethyl acetate (20 mL), the mixture was washed with water (20 mL) and saturated brine (20 mL) and dried with anhydrous sodium sulfate, followed by distilling off of the solvent under reduced pressure. The residue was purified using silica gel flash column chromatography (hexane:ethyl acetate, 8:1-5:1, V/V) to obtain a colorless oil (307 mg, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361744B2
Source datasetuspto-grants-2008_04
ORD IDord-1b7a47853b3d4d689b63ed7eb2b3d2fe
Source noteuspto-grants-2008_04