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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

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 (4.6g; 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04082851
Source datasetuspto-grants-1978_04
ORD IDord-83b17e5f3e5b4e04bc96747c35c99305
Source noteuspto-grants-1978_04