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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725667Generated: November 2, 2026

Ammonium Hydroxide → HCID 57562895, compound

https://huagongshe.com/reaction/1725667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant2-Fluoro-3-methyl-5-nitrobenzene-1-sulfonyl chlorideHCID 57562880—
SolventEthyl AcetateHCID 8857—
ProductHCID 57562895HCID 57562895—

Reaction Steps

The resulting oily residue of compound 26 was taken up in ethyl acetate (100 mL) and stirred with ammonium hydroxide (100 mL, 30% aqueous solution) overnight at room temperature. After the ethyl acetate layer was separated, the aqueous layer was extracted with ethyl acetate (2×50 mL). The organic layers were combined, dried over anhydrous sodium sulfate and the solvent was removed under vacuum. The dark oily residue was chromatographed (silica gel, hexanes then 10%, 20%, up to 50% ethyl acetate in hexanes to afford 3-aminosulfonyl-4-fluoro-5-methylnitrobenzene (27). LCMS: purity: 89%; MS (m/z): 235 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491732B2
Source datasetuspto-grants-2009_02
ORD IDord-aaae855d4a2c41349957d8a7597ac04a
Source noteuspto-grants-2009_02