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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743342Generated: November 1, 2026

Hydrochloric Acid → HCID 22239063, compound

https://huagongshe.com/reaction/1743342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
ReactantIsophthaloyl chlorideHCID 7451—
Reactant2',6'-DihydroxyacetophenoneHCID 69687—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22239063HCID 22239063—

Reaction Conditions

Temperature-10 °C

Reaction Steps

Dry, pulverulent lithium hydroxide (19.5 mmol, 3 equivalents) is added in one portion to a well-stirred solution of 2,6-dihydroxyacetophenone (6.6 mmol) in dry THF (5 ml) under an argon atmosphere at −78° C. The reaction mixture is stirred at −78° C. for one hour and subsequently at −10° C. for two hours. After the mixture has been re-cooled to −78° C., a solution of isophthaloyl chloride (3.3 mmol) in THF (10 ml) is added in one portion. The mixture is stirred at −78° C. for one hour and at room temperature for 4 hours until the starting material has disappeared. The reaction mixture is emptied into a mixture of ice (150 g) and concentrated HCl (5 ml) and extracted with chloroform (3×50 ml). The solvents are removed from the dried extracts, and the residue is dried under reduced pressure for 24 hours. Glacial acetic acid (30 ml) and sulfuric acid (0.2 ml) are added to the residue, and the mixture is heated at 95–100° C. for from 30 minutes to one hour under an argon atmosphere. Approximately one third of the acetic acid is stripped off, and the residue is emptied into water. The precipitated product is filtered, washed and dried and recrystallised in methanol, giving 3′-(5-hydroxychromonyl)-5-hydroxyflavone. EI-MS (70 eV) m/e (rel. abund.)=398.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07009062B2
Source datasetuspto-grants-2006_03
ORD IDord-b8ff7ff02f764b0bb14ba6a338f66697
Source noteuspto-grants-2006_03