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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62631Generated: October 30, 2026

Trifluoroacetic acid → HCID 118271394, compound

https://huagongshe.com/reaction/62631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantBenzyl(methoxymethyl)((trimethylsilyl)methyl)amineHCID 353442—
Reactant(1E)-2-(3,5-dichlorophenyl)-3,3,3-trifluoroprop-1-en-1-yl phenyl sulfoxideHCID 118340468—
SolventTolueneHCID 1140—
ProductHCID 118271394HCID 11827139483%

Reaction Steps

Trifluoroacetic acid (38 μL, 513 μmol) was added to (1E)-2-(3,5-dichlorophenyl)-3,3,3-trifluoroprop-1-en-1-yl phenyl sulfoxide (4.00 g, 98% purity, 10.3 mmol) in toluene (20 mL). N-Benzyl-1-methoxy-N-[(trimethylsilyl)methyl]methanamine (3.65 g, 15.4 mmol) in toluene (18 mL) was added at room temperature over two hours. After two more hours additional N-Benzyl-1-methoxy-N-[(trimethylsilyl)-methyl]methanamine (0.2 eq.) was added and the reaction left stirring for another hour. The solvents of the reaction mixture were removed and the crude product was taken up in n-heptane. The formed crystals were filtered off. 1-Benzyl-3-(3,5-dichlorophenyl)-4-(phenylsulfinyl)-3-(trifluoromethyl)-pyrrolidinium chloride (4.40 g, >99% purity, 83% yield, E/Z [not assigned]=53/47) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447036B2
Source datasetuspto-grants-2016_09
ORD IDord-5d8151d018c746e5b2acf2b6b052a358
Source noteuspto-grants-2016_09