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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904542Generated: November 1, 2026

HCID 12760922, compound → HCID 15729797, compound

https://huagongshe.com/reaction/1904542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 12760922HCID 12760922—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductHCID 15729797HCID 1572979786%

Reaction Steps

A 100 ml autoclave was charged with 6.0 g of 7-hydroxy-2,4,4-trimethyl-4H-1-benzopyran synthesized by the method of Japanese Laid-Open Patent Publication No. 5475/1981, 1.0 g of 5% palladium-carbon and 20 ml of ethanol, and hydrogenation was carried out at 85° C. The resulting product was recrystallized from n-hexanetoluene to give 5.2 g (86%) of the desired product as colorless crystals (melting point 97°-98° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04838924
Source datasetuspto-grants-1989_06
ORD IDord-e6c2435877674706ba3cd34d5a9826bf
Source noteuspto-grants-1989_06