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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Urea, (1,2,3,4-tetrahydro-4-oxo-1-naphthalenyl)- | HCID 3628438 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,2,3,4-Tetrahydro-4-hydroxy-1-naphthylurea | HCID 4294518 | 11.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04089976 |
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| Source dataset | uspto-grants-1978_05 |
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| ORD ID | ord-3f023918618e4006ac626d1d7ebe2c94 |
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| Source note | uspto-grants-1978_05 |
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