HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-2-nitrobenzene → Benzenesulfonyl chloride, 4-chloro-3-nitro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-2-nitrobenzene | HCID 6945 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Product | Benzenesulfonyl chloride, 4-chloro-3-nitro- | HCID 7323 | — |
Reaction Steps
On the other hand, those compounds of formula (1) wherein X is hydroxy and A is a sulfonamido group can be prepared by treating, for example, ortho-nitro-chlorobenzene with chlorosulfonic acid to obtain 3-nitro-4-chlorobenzenesulfonylchloride, followed by treatment with a primary or secondary amine to yield the corresponding 3-nitro-4-chlorobenzene sulfonamido derivative. This product is then treated with caustic soda to yield the 3-nitro-4-hydroxybenzene sulfonamide and subsequently reduced to the desired 3-amino-4-hydroxybenzene sulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04058515 |
| Source dataset | uspto-grants-1977_11 |
| ORD ID | ord-4a148da3133d49b69d8014ccc090331b |
| Source note | uspto-grants-1977_11 |