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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072145Generated: October 30, 2026

Ethanol → 1,2,3,4-Tetrahydro-4-hydroxy-1-naphthylurea

https://huagongshe.com/reaction/2072145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantUrea, (1,2,3,4-tetrahydro-4-oxo-1-naphthalenyl)-HCID 3628438—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
Product1,2,3,4-Tetrahydro-4-hydroxy-1-naphthylureaHCID 4294518—

Reaction Steps

To a stirred solution of 4.6 g. of 1,2,3,4-tetrahydro-4-oxo-1-naphthylurea in 230 ml. of ethanol 0.85 g. of sodium borohydride is added. The reaction mixture is stirred for about 5 hours and after standing overnight 50 ml. water is added while stirring. The mixture is then evaporated in vacuo to remove the solvent. Water (50 ml.) is added, then glacial acetic acid is added, until the foaming caused by the acid ceases. The solution is evaporated to dryness in vacuo, alcohol is added and the whole evaporated to dryness in vacuo. Then 30 ml. of ethanol is added to the residue and the mixture stirred and filtered. The collected insoluble solid is air dried. This solid is heated with 300 ml. of acetone and filtered. The filtrate is concentrated in vacuo to afford 0.55 g. of the title compound, melting point 170°- 176° C. On further work-up of the acetone mother liquor, 0.2 g. of the title compound, melting point 169°-174° C., is recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04049717
Source datasetuspto-grants-1977_09
ORD IDord-ce7ae1f82271401b9f3638504a8de9e9
Source noteuspto-grants-1977_09