Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056825Generated: October 30, 2026

Hydrochloric Acid → HCID 86713228, compound

https://huagongshe.com/reaction/1056825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPiperidineHCID 8082—
ReactantTriisopropyl borateHCID 21531—
ReactantSodium BicarbonateHCID 516892—
ReactantBoron monoxideHCID 6327189—
ReactantHCID 86713229HCID 86713229—
ReactantHCID 86713230HCID 86713230—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 86713228HCID 8671322870%

Reaction Conditions

Temperature70 °C

Reaction Steps

In a 20 mL reaction vessel were placed 31.0 mg (136 μmol) of 6-(1H-indol-4-yl)hex-5-ene-2,4-dione and 13.2 mg (0.190 mmol) of boron oxide and they were dissolved in 0.88 mL of ethyl acetate. To the mixture under stirring at 70° C., 33 mg (0.14 mmol) of 2-methoxy-4-(3-pyridylmethoxy)benzaldehyde and 62 μL (0.27 mmol) of triisopropyl borate were sequentially added. After the mixture was stirred at the same temperature for 1 hour, a solution of 2.7 μL (27 μmol) of piperidine in ethyl acetate (0.135 mL) was added and the mixture was further stirred for 1 hour. To the reaction mixture was added a 1:1 solution (0.4 mL) of 1 N hydrochloric acid and saturated brine at room temperature and the mixture was stirred for 5 minutes to 1 hour (further, the mixture was neutralized with a saturated sodium bicarbonate aqueous solution as needed). The resulting organic phase was directly subjected to purification by silica gel column chromatography (hexane/ethyl acetate or methylene chloride/methanol) to give 42.8 mg (70% yield) of the title compound as an orange powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399635B2
Source datasetuspto-grants-2016_07
ORD IDord-a282338b6e4342d8a29043f01814b0a0
Source noteuspto-grants-2016_07