HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249280Generated: October 30, 2026
Hydrochloric Acid → 3-(Isopropylsulfonyl)amino-4-nitrobenzophenone
https://huagongshe.com/reaction/1249280
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Propane-2-sulfonamide | HCID 3549191 | — |
| Reactant | (3-Fluoro-4-nitrophenyl)(phenyl)methanone | HCID 13363147 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 3-(Isopropylsulfonyl)amino-4-nitrobenzophenone | HCID 13363148 | 95% |
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 lN 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04629811 |
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| Source dataset | uspto-grants-1986_12 |
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| ORD ID | ord-5e5b9ed834a64262bee328a6327db6cc |
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| Source note | uspto-grants-1986_12 |
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