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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45407Generated: October 26, 2026

Potassium Nitrate → 4-(Ethylsulfonyl)-1-fluoro-2-nitrobenzene

https://huagongshe.com/reaction/45407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium NitrateHCID 24434—
ReactantFluoresoneHCID 71814—
SolventSulfuric AcidHCID 1118—
Product4-(Ethylsulfonyl)-1-fluoro-2-nitrobenzeneHCID 6736026366%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 1-(ethylsulfonyl)-4-fluorobenzene (1.36 mmol, 0.257 g) in sulfuric acid (1.32 ml) was added potassium nitrate (0.243 g) at 80° C. The mixture was stirred at 90° C. for 2 hours. Ice water (5 ml) was added and the mixture was extracted with ethyl acetate (25 ml) and washed with water (20 ml) and brine (10 ml). The organic extracts were combined and dried over sodium sulfate and concentrated. The residue was purified by column chromatography (hexane/ethylacetate 1:3) to give a light yellow solid which was crystallized from methanol. HPLC indicated 98% purity, mp 128-131° C., (0.21 g, 66% yield). 1H NMR (CDCl3): 1.35 (t, 3H, CH3), 3.21 (q, 2H, CH2), 7.55 (t, 1H, Ar—H), 8.21 (m, 1H, Ar—H), 8.64 (d, 1H, Ar—H); MS: 229 M−. Elemental Analysis (C, H, N, F, S) for C8H8FNO4S; calculated C, 41.20; H, 3.46; N, 6.01; F, 8.15; S, 13.75. found C, 41.31; H, 3.35; N, 5.85; F, 8.17; S, 13.53.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541476B2
Source datasetuspto-grants-2013_09
ORD IDord-f71feadad67f41ecaa39e431e9b6e979
Source noteuspto-grants-2013_09