Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868182Generated: November 1, 2026

Trifluoromethanesulfonic acid → HCID 67157467, compound

https://huagongshe.com/reaction/1868182

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 numberUS07632930B2
Source datasetuspto-grants-2009_12
ORD IDord-85ee4d72ebf947ec9ba62ecfdc0948d0
Source noteuspto-grants-2009_12