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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979972Generated: October 30, 2026

Hydrochloric Acid → 3-(Isopropylsulfonyl)amino-4-nitrobenzophenone

https://huagongshe.com/reaction/1979972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantPropane-2-sulfonamideHCID 3549191—
Reactant(3-Fluoro-4-nitrophenyl)(phenyl)methanoneHCID 13363147—
SolventDimethyl SulfoxideHCID 679—
Product3-(Isopropylsulfonyl)amino-4-nitrobenzophenoneHCID 1336314895%

Reaction Steps

To 50 ml. of dimethylsulfoxide (DMSO) was added 1.01 g. (0.021 m.) of 50% sodium hydride in oil. After the initial gas evolution ceased, 2.53 g. (0.0206 m.) of isopropylsulfonamide [prepared according to Duguet, Rec. Trav. Chim., 25, 215 (1906)] was added. The mixture was stirred under a calcium chloride drying tube for ten minutes after which time 4.90 g. (0.020 m.) of 3-fluoro-4-nitrobenzophenone was added, followed by 20 ml. of DMSO. After stirring for five hours at room temperature, the reaction solution was poured into a mixture of ice and 1N hydrochloric acid which was then extracted several times with ethyl acetate. The extracts were combined, washed with water, and dried over magnesium sulfate. The oil remaining after evaporation was triturated with isopropanol to give 6.65 g. (95% yield) of 3-(isopropylsulfonyl)amino-4-nitrobenzophenone as a yellow powder. Crystallization from isopropanol gave pale yellow needles, m.p. about 115°-116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04483986
Source datasetuspto-grants-1984_11
ORD IDord-7faa5467792b4d498191252ec7a1279d
Source noteuspto-grants-1984_11