Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596306Generated: October 28, 2026

Benzene → HCID 21451984, compound

https://huagongshe.com/reaction/596306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 21451997HCID 21451997—
ProductHCID 21451984HCID 21451984—

Reaction Steps

To a mixture of 0.35 g of lithium aluminum hydride and 15 ml of tetrahydrofuran, there was added dropwise a solution of 2.05 g of 3-{2-(2-ethoxyphenoxy)ethylamino}-p-fluoropropionanilide in 20 ml of tetrahydrofuran. Then, the resulting mixture was refluxed for 3 hours. To the reaction mixture cooled in ice, there were gradually added water and benzene. The organic layer was separated, dried over sodium sulfate and evaporated under reduced pressure. The oily residue was dissolved in isopropanol, and a warm solution of 0.8 g of oxalic acid in 10 ml of isopropanol was added thereto. After cooling, the precipitate was collected by filtration and dried to give N-{2-(2-ethoxyphenoxy)ethyl}-3-(4-fluoroanilino)propylamine hydrogen oxalate, M.P. 193°-196° C (decomp.). Recrystallization from methanol gave white crystals, M.P. 218°-219° C (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04010280
Source datasetuspto-grants-1977_03
ORD IDord-49fa7b5a4cb4430c9f159a618fbfc638
Source noteuspto-grants-1977_03