HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579743Generated: November 3, 2026
2,5-Dichloronitrobenzene → 2,5-Dichloroaniline
https://huagongshe.com/reaction/1579743
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,5-Dichloronitrobenzene | HCID 6977 | — |
| Reactant | Sodium hydrogen sulphide | HCID 86586439 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,5-Dichloroaniline | HCID 7262 | — |
Reaction Steps
576 Parts of 2,5-dichloro-nitrobenzene and 300 parts of water were placed in a stirring apparatus and reacted in the same manner as described in Example 1 with 1,446 parts of a 36% sodium hydrogen sulfide solution at a temperature within the range of from 80° to 85°C. Then, the 2,5-dichloroaniline formed as by-product was separated by steam distillation. After cooling to 20°C 1,210 parts of sodium sulfite and 430 parts of xylene were successively added and the pH was adjusted at 6 at a temperature within the range of from 8° to 12°C during 3 to 4 hours with 550 parts of 30% hydrochloric acid while stirring. After precipitation and separation of the organic phase, the aqueous phase was stirred once with 174 parts of xylene. 4-Chloro-2-amino-thiophenol was isolated from the organic phase, combined by vacuum distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03931321 |
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| Source dataset | uspto-grants-1976_01 |
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| ORD ID | ord-6fa69c23e5ad44909318ee3626106a75 |
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| Source note | uspto-grants-1976_01 |
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