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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390055Generated: November 1, 2026

Pyridine → 5-Formyl-3-(methylamino)-2-phenoxybenzene-1-sulfonamide

https://huagongshe.com/reaction/1390055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
Reactant5-(Hydroxymethyl)-3-(methylamino)-2-phenoxybenzene-1-sulfonamideHCID 54137754—
SolventAcetoneHCID 180—
Product5-Formyl-3-(methylamino)-2-phenoxybenzene-1-sulfonamideHCID 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 (4.6 g; prepared as described in Example 5) in acetone (25 ml) is then added in one portion and the mixture is stirred 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04247550
Source datasetuspto-grants-1981_01
ORD IDord-124b18f48a554e7fbdffd015d1262397
Source noteuspto-grants-1981_01