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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489272Generated: November 1, 2026

HCID 18707311, compound → HCID 18707291, compound

https://huagongshe.com/reaction/1489272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18707311HCID 18707311—
ReactantHCID 178418435HCID 178418435—
SolventMethanolHCID 887—
ProductHCID 18707291HCID 1870729199.5%

Reaction Steps

In 20 ml of methanol was suspended 300 mg of 2-(3,4- diethoxyphenyl)-4-(3-methoxycarbonyl-4-hydroxy-5-formylphenyl)thiazole with stirring. Threto was added 26.5 mg of sodium boron hydride at 0° C. The mixture was stirred at room temperature for 1 hour. 26.5 mg of sodium boron hydride was further added, and the resulting mixture was stirred at the same temperature for 1 hour. The solvent was removed from the reaction mixture by distillation. To the residue were added 30 ml of dichloromethane and 15 ml of water, and phase separation was conducted. The organic layer was washed with 10 ml of a saturated aqueous sodium chloride solution, dried and subjected to distillation to remove the solvent to obtain 300 mg of 2-(3,4-diethoxyphenyl)-4-(3-methoxycarbonyl-4-hydroxy-5-hydroxymethylphenyl)thiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05677319
Source datasetuspto-grants-1997_10
ORD IDord-42a2207be2b9444da22245c08ff37763
Source noteuspto-grants-1997_10