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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant1-Chloro-2-nitro-4-trifluoromethanesulfonylbenzeneHCID 1547956—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-Nitro-4-((trifluoromethyl)sulfonyl)phenolHCID 503518725.1%

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426443B2
Source datasetuspto-grants-2013_04
ORD IDord-1cb5ed129a424bb29431cd0f3f40041f
Source noteuspto-grants-2013_04