Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854651Generated: October 26, 2026

Hydrochloric Acid → HCID 68551550, compound

https://huagongshe.com/reaction/1854651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantButylamineHCID 8007—
ReactantIsovanillinHCID 12127—
ReactantTributyl borateHCID 12712—
ReactantSodium BicarbonateHCID 516892—
ReactantBoron trioxideHCID 518682—
Reactant6-(4-Hydroxyphenyl)hex-5-ene-2,4-dioneHCID 67106734—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 68551550HCID 6855155086.2%

Reaction Steps

6-(4-Hydroxyphenyl)hex-5-ene-2,4-dione (17.5 mg, 85 μmol) and boron trioxide (11 mg, 0.16 mmol) was placed in a 20 mL reaction vessel, and dissolved in 0.4 mL of ethyl acetate. To the stirring mixture at 80° C. was added a solution of 3-hydroxy-4-methoxybenzaldehyde (16 mg, 0.11 mmol) and tri-n-butyl borate (25 μL, 93 μmol) in 0.7 mL of ethyl acetate. After the reaction mixture was stirred for 2 h at the same temperature, n-butylamine (10 μL, 0.10 mmol) was added with additional stirring for 1 h. The reaction mixture was treated with a 1:1 solution of 1N HCl and brine, and was stirred at 50° C. for 5 min to 1 h (if necessary, the reaction mixture was neutralized by saturated NaHCO3 aqueous solution). The organic layer was purified directly by silica gel column chromatography (eluting with hexane/ethyl acetate or chloroform/methanol) to obtain the title compound (24.8 mg, 86%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962674B2
Source datasetuspto-grants-2015_02
ORD IDord-8b4cf491f9544925bd1f0b7b16c6b61f
Source noteuspto-grants-2015_02