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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589181Generated: November 2, 2026

Tetrahydrofuran → N-[3-(1H-imidazol-1-yl)propyl]-2-phenoxyacetamide

https://huagongshe.com/reaction/1589181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPhenoxyacetic AcidHCID 19188—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3-(Imidazole-1-yl)-propylamine DihydrochlorideHCID 12250969—
SolventWaterHCID 962—
ProductN-[3-(1H-imidazol-1-yl)propyl]-2-phenoxyacetamideHCID 5081968—

Reaction Steps

A mixture of 2.28 g. of phenoxyacetic acid, 2.43 g. of 1,1'-carbonyldiimidazole and 50 ml. of tetrahydrofuran was stirred at room temperature for 2 hours, then 3.0 g. of 1H-imidazole-1-propanamine dihydrochloride was added. The reaction mixture was stirred for 18 hours, then heated at reflux temperature for 5 hours, 5 ml. of water was added, the mixture was heated for 30 minutes and then concentrated to remove the tetrahydrofuran. The residue was treated with methylene chloride and 50 ml. of 1N sodium hydroxide and the layers separated. The organic layer was washed with water, dried over magnesium sulfate and concentrated. The residue was washed onto a filter with ether, giving the desired product, m.p. 91°-93° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04568687
Source datasetuspto-grants-1986_02
ORD IDord-de6934bdb7514aa2bab718b2e63cf2d8
Source noteuspto-grants-1986_02