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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901789Generated: October 31, 2026

Trifluoromethanesulfonic acid → HCID 67157834, compound

https://huagongshe.com/reaction/901789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantBenzyl 2,2,2-trichloroacetimidateHCID 144968—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67157096HCID 67157096—
SolventEthyl AcetateHCID 8857—
SolventDichloromethane cyclohexaneHCID 21916607—
ProductHCID 67157834HCID 67157834112.5%

Reaction Steps

The compound (3.37 g, 9.07 mmol) synthesized in Example 1 (1h) was dissolved in methylene chloride:cyclohexane (1:2, 180 mL) and benzyl trichloroacetoimidate (2.0 mL, 10.88 mmol) and trifluoromethanesulfonic acid (2.57 mL, 15.3 mmol) were added thereto, followed by stirring of the mixture at room temperature for 1 hour. After saturated aqueous sodium hydrogencarbonate solution (20 mL) was added to the reaction mixture at 0° C. and the mixture was diluted with ethyl acetate (200 mL), it was washed with water (300 mL) and saturated aqueous sodium hydrogencarbonate solution (300 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, 5:1-2:1, V/V) to obtain 4.71 g of pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361744B2
Source datasetuspto-grants-2008_04
ORD IDord-51cb822a21be45a88d33dc5d4d24f028
Source noteuspto-grants-2008_04