HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082877Generated: October 31, 2026
Pyridine → 5-Formyl-3-(methylamino)-2-phenoxybenzene-1-sulfonamide
https://huagongshe.com/reaction/2082877
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 5-(Hydroxymethyl)-3-(methylamino)-2-phenoxybenzene-1-sulfonamide | HCID 54137754 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 5-Formyl-3-(methylamino)-2-phenoxybenzene-1-sulfonamide | HCID 20294632 | — |
Reaction Steps
To a stirred mixture of dry pyridine (15 ml) and dry methylene chloride (225 ml), chromic anhydride (9.0 g) is added in one portion, and the mixture is stirred for 15 minutes. A solution of 3-methylamino-4-phenoxy-5-sulfamylbenzyl alcohol (4.6g; prepared as described in Example 5) in acetone (25 ml) is then added in one portion and the mixture is stired for a further 15 minutes. The resulting inorganic precipitate is removed by filtration and the filtrate is evaporated in vacuo. The residue is extracted with diethyl ether (300 ml) and filtered to remove a small amount of insoluble material. The diethyl ether is removed in vacuo to yield crude 3-methylamino-4-phenoxy-5-sulfamylbenzaldehyde. After recrystallization from ethanol it is obtained with a melting point of 166°-167° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04082851 |
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| Source dataset | uspto-grants-1978_04 |
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| ORD ID | ord-83b17e5f3e5b4e04bc96747c35c99305 |
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| Source note | uspto-grants-1978_04 |
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