HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968974Generated: October 31, 2026
Hydrochloric Acid → 2-Nitro-4-((trifluoromethyl)sulfonyl)phenol
https://huagongshe.com/reaction/1968974
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Chloro-2-nitro-4-trifluoromethanesulfonylbenzene | HCID 1547956 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Nitro-4-((trifluoromethyl)sulfonyl)phenol | HCID 5035187 | 25.1% |
Reaction Steps
Sodium hydroxide (211 mg, 5.28 mmol) was added to a suspension of 1-chloro-2-nitro-4-[(trifluoromethyl)sulfonyl]benzene (297 mg, 1.03 mmol) in H2O (5 mL) at rt, followed by methanol (0.5 mL) to solubilise the starting material, and the reaction was heated at 110° C. for 1 h. The mixture was allowed to cool to rt, diluted with H2O (10 mL) and neutralised with 5 M HCl. DCM was added, the 2 layers were partitioned and the aqueous layer was extracted with DCM (2×). The combined organics were dried (Na2SO4) and concentrated by rotary evaporation to give 2-nitro-4-[(trifluoromethyl)sulfonyl]phenol (D82, 70 mg, 25%) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08426443B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-1cb5ed129a424bb29431cd0f3f40041f |
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| Source note | uspto-grants-2013_04 |
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