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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337343Generated: October 29, 2026

2-Aminoresorcinol ditosylate → 2-(3,5-Dimethyl-1H-pyrazol-1-yl)-3-hydroxyphenyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/337343

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Aminoresorcinol ditosylateHCID 86703253—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventSodium NitriteHCID 23668193—
Product2-(3,5-Dimethyl-1H-pyrazol-1-yl)-3-hydroxyphenyl 4-methylbenzenesulfonateHCID 8670325454.7%

Reaction Steps

To 278 mg of 2-amino-1,3-phenylene bis(4-methylbenzene sulfonate) was added 0.64 ml of 5N-hydrochloric acid, and to the mixture a solution in which 58 mg of sodium nitrite was dissolved in 0.4 ml of water was added dropwise at 0° C., and stirred for 30 minutes. Then, a solution in which 289 mg of stannous chloride was dissolved in 0.32 ml of 5N-hydrochloric acid was added dropwise at 0° C. and stirred for 1 hour. The solvent was distilled off under reduced pressure, and 1.3 ml of ethanol and 66 μl of acetyl acetone were added and heated at reflux for 2 hours. To the reaction mixture was added 50 ml of water, and neutralized with a saturated sodium bicarbonate solution and extracted with 50 ml of ethyl acetate. After the organic layer was dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure, and purified using silica gel column chromatography (hexane:ethyl acetate=4:1 to 1:1) to yield 62.9 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889727B2
Source datasetuspto-grants-2014_11
ORD IDord-c76a3cc9afb64337ba027a8af58cd767
Source noteuspto-grants-2014_11