HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374875Generated: October 28, 2026
Dichloromethane → 2-Chloro-5-(phenylsulphonyl)aniline
https://huagongshe.com/reaction/374875
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 1-Chloro-2-nitro-4-(phenylsulfonyl)benzene | HCID 580489 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Chloro-5-(phenylsulphonyl)aniline | HCID 3020773 | 82.8% |
Reaction Steps
2-Nitro-4-(phenylsulfonyl)chlorobenzene (9.8 g) and stannous chloride dihydrate (33.5 g) were suspended in absolute ethanol (200 mL) and heated to 75° C. for 40 minutes. The solution was evaporated and the resulting material was cooled to 0° C. Water (100 mL) was added, and the pH was adjusted to 8.0 with aqueous sodium hydroxide. The resulting solids were removed by filtration and the aqueous filtrate was extracted with ethyl acetate. The combined ethyl acetate solutions were evaporated to give a brown solid. Chromatography, with dichloromethane as the eluent yielded the aniline as an orange solid (7.3 g); mp: 105°-107° C.; 250 MHz NMR: 5.96 (s,2), 7.02 (dd,1 J=8, 2), 7.34 (d,1, J=2), 7.41 (d,1, J=8), 7.61 (m,3), 7.88 (d,2, J=7); MS: m/z=268(M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05482969 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-b82f3e4454414af581996391e6285189 |
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| Source note | uspto-grants-1996_01 |
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