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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372273Generated: October 29, 2026

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

https://huagongshe.com/reaction/372273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantUrea, (1,2,3,4-tetrahydro-4-oxo-1-naphthalenyl)-HCID 3628438—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
Product1,2,3,4-Tetrahydro-4-hydroxy-1-naphthylureaHCID 429451811.8%

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 numberUS04089976
Source datasetuspto-grants-1978_05
ORD IDord-3f023918618e4006ac626d1d7ebe2c94
Source noteuspto-grants-1978_05