HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693145Generated: October 31, 2026
Trifluoromethanesulfonic acid → HCID 67476460, compound
https://huagongshe.com/reaction/1693145
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 67279256 | HCID 67279256 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 67476460 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158620B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-0d00610e56e9450f9e038202e1b41490 |
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| Source note | uspto-grants-2012_04 |
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