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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309699Generated: October 31, 2026

Fumaric Acid → HCID 131715266, compound

https://huagongshe.com/reaction/2309699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFumaric AcidHCID 444972—
ReactantHCID 131715267HCID 131715267—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 131715266HCID 131715266—

Reaction Steps

A solution of 27.27 g of N-(2,6-dimethylphenyl)-1H-imidazole-butanamide hydrobromide salt in 250 ml of dry tetrahydrofuran was added dropwise with stirring to 530 ml of 1 molar borane in tetrahydrofuran and the resulting solution was heated to reflux for 2 hours. After cooling, excess methanol was added to decompose the remaining borane and the solution was evaporated to dryness. The residue was acidified by the cautious addition of 285 ml of 2N hydrochloric acid and was warmed on the steam bath for 20 minutes. The resulting solution was cooled, made strongly basic with sodium hydroxide solution and was extracted with dichloromethane. The combined organic layers were dried with potassium carbonate and concentrated to give 25.1 g of N-(2,6-dimethylphenyl)-1H-imidazole-1-butanamine as an oil which was dissolved in 200 ml of methanol, treated with 23.9 g of fumaric acid and diluted with 600 ml of ether. The resulting solid amounted to 37.0 g of N-(2,6-dimethylphenyl)-1H-imidazole-1-butanamide (E)-2-butenedioate(1:2) salt, mp 146°-147° C. Recrystallization from methanol-ether gave the analytical sample, mp 148°-149° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04696930
Source datasetuspto-grants-1987_09
ORD IDord-2ac10125f6564ab896ddd84c217fed9e
Source noteuspto-grants-1987_09