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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583428Generated: October 31, 2026

N-[4-(1H-Imidazol-1-yl)butyl]formamide → 4-(1H-Imidazol-1-yl)-N-methylbutan-1-amine

https://huagongshe.com/reaction/1583428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[4-(1H-Imidazol-1-yl)butyl]formamideHCID 13557541—
SolventTetrahydrofuranHCID 8028—
Product4-(1H-Imidazol-1-yl)-N-methylbutan-1-amineHCID 1355754068%

Reaction Steps

A solution of 58.8 g of N-[4-(1H-imidazol-1-yl)butyl]formamide in 480 ml of dry tetrahydrofuran was treated with 87.0 ml of 10 Molar borane methyl sulfide complex in tetrahydrofuran. The reaction mixture was heated to reflux for 18 hours under an argon atmosphere, cooled in an ice bath and quenched with 400 ml of methanol. The solvent was removed, the methanol addition and evaporation repeated, and the residue was made acidic with hydrochloric acid and was stirred over night. The mixture was made basic with sodium hydroxide solution and was extracted with dichloromethane. The combined organic layers were dried over potassium carbonate and evaporated to give an oil which was distilled to give 35.9 g (68%) of 4-(1H-imidazol-1-yl)-N-methylbutanamine, bp 130°-135° C./0.3 mm. The product was further characterized as the picrate, mp 111-113.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04551460
Source datasetuspto-grants-1985_11
ORD IDord-4403d35c0e074fb4896d16a2efb5da5e
Source noteuspto-grants-1985_11