HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697617Generated: November 1, 2026
Triethylamine → 1-Ethenesulfonyl-2-trifluoromethyl-benzene
https://huagongshe.com/reaction/1697617
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(2-Bromo-ethylsulfonyl)-2-trifluoromethyl-benzene | HCID 66770999 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Ethenesulfonyl-2-trifluoromethyl-benzene | HCID 23466718 | 84.2% |
Reaction Steps
To a stirred solution of 1-(2-bromo-ethylsulfonyl)-2-trifluoromethyl-benzene (5.4 g, 19 mmol) in dichloromethane (50 ml) was added triethylamine (4.66 ml, 34 mmol). The reaction mixture was heated under reflux conditions to 50° C. for 12 h. The solvent was removed under reduced pressure and the residue was purified by column chromatography (silica gel, EtOAc/heptane) to yield the title compound (3.68 g, 16 mmol; 69%) as off-white semi-solid. MS (ESI): m/z=254.1 [M+NH4]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163793B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-a8774a72758746ab8c7daaea1f903e8d |
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| Source note | uspto-grants-2012_04 |
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