HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326709Generated: October 25, 2026
4-Methoxybenzenesulfonyl chloride → 4-Methoxybenzenesulfonamide
https://huagongshe.com/reaction/326709
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Methoxybenzenesulfonamide | HCID 70789 | — |
Reaction Steps
25 ml of 25% NH4OH were added dropwise while cooling in an ice bath to a solution of 7.3 g of p-methoxybenzenesulfonyl chloride in 50 ml of tetrahydrofuran. Subsequently, the reaction mixture was stirred vigorously for 30 minutes at 70° C. (bath temperature). Thereafter, the tetrahydrofuran was distilled. The residue was extracted with ethyl acetate. There was obtained p-methoxybenzenesulfonamide which was converted into the potassium salt as described in Example 50.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05270313 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-951efbaa19c74b62ab9164d05a2e3923 |
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| Source note | uspto-grants-1993_12 |
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