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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578854Generated: November 4, 2026

Furfural → HCID 54430759, compound

https://huagongshe.com/reaction/1578854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFurfuralHCID 7362—
ReactantHCID 21558938HCID 21558938—
ProductHCID 54430759HCID 54430759—

Reaction Steps

The starting material is prepared as follows: The mixture of 3.5 g of 4-phenoxy-3-amino-5-(2-acetamidophenylsulfamoyl)-benzoic acid and 30 ml of furfural is heated to 100° for five hours and allowed to stand at room temperature for 16 hours. It is evaporated under reduced pressure, the residue triturated with diethyl ether and dissolved in 75 ml of ethanol. Thereupon 2 g of sodium borohydride are added while stirring and cooling followed by another 0.5 g thereof after 4 hours and another 0.5 g thereof after 16 hours and stirring is continued for one hour. Thereupon 100 ml of water are added, the mixture filtered and the filtrate acidified with hydrochloric acid to a pH of 2-3. The precipitate formed is filtered off and recrystallized from 30% aqueous ethanol to yield the 4-phenoxy-3-furfurylamino-5-(2-acetamidophenylsulfamoyl)-benzoic acid melting at 207°-210° with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03939267
Source datasetuspto-grants-1976_02
ORD IDord-b77d95e30d534825afe4f69f15bf2656
Source noteuspto-grants-1976_02