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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166153Generated: October 26, 2026

HCID 178515562, compound → HCID 178515560, compound

https://huagongshe.com/reaction/1166153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178515562HCID 178515562—
CatalystNickelHCID 935—
SolventAmmoniaHCID 222—
ProductHCID 178515560HCID 17851556055.2%

Reaction Steps

To 2-mercapto-6-hydroxy-4-phenylpyrimidine (10 g) in ‘880’ ammonia solution (100 ml) was carefully added Raney nickel (32.5 g, 50% slurry) portionwise. Immediate effervescence took place. The mixture was heated to reflux for 4 hours, filtered and concentrated under reduced pressure. The initial residue was azeotroped with toluene (×2) to remove final traces of water. The pale blue residue was dissolved in hot ethanol and filtered and then the filtrate was treated with charcoal. The resulting green solution was evaporated under reduced pressure to afford crude 4-hydroxy-6-phenylpyrimidine (4.65 g) as a green solid (m.p.>300° C.) which was used in the next stage without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613773B2
Source datasetuspto-grants-2003_09
ORD IDord-d059d81e8b8149fb9ec006643731c64c
Source noteuspto-grants-2003_09