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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693145Generated: October 31, 2026

Trifluoromethanesulfonic acid → HCID 67476460, compound

https://huagongshe.com/reaction/1693145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67279256HCID 67279256—
SolventDiethyl EtherHCID 3283—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 67476460HCID 67476460—

Reaction Steps

2-[2-(2-Fluorophenyl)cyclohex-1-enylmethyl]isothiourea hydrochloride obtained in Preparation Example 1-(5) (6.38 g) was dissolved in TFA (32.0 mL) under ice-cooling, and trifluoromethanesulfonic acid (6.40 mL) was added dropwise at the same temperature. The reaction solution was stirred overnight with gradual warming to room temperature. The reaction solution was poured into ice, diluted with diethyl ether and then neutralized with sodium bicarbonate. The generated reaction mixture was extracted with ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate. The drying agent was removed by filtration and the filtrate was concentrated under reduced pressure to obtain a crude product. The crude product was purified by NH-silica gel column chromatography to obtain the title compound (4.58 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158620B2
Source datasetuspto-grants-2012_04
ORD IDord-0d00610e56e9450f9e038202e1b41490
Source noteuspto-grants-2012_04