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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390263Generated: October 30, 2026

Hydrochloric Acid → HCID 53838878, compound

https://huagongshe.com/reaction/1390263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantHydrazine, (3,4-dimethoxyphenyl)-, hydrochlorideHCID 88490—
Reactant1-(4,4-Diethoxybutyl)piperidin-2-oneHCID 3017372—
SolventEthanolHCID 702—
ProductHCID 53838878HCID 5383887821.7%

Reaction Steps

One dissolves 54 g of 3,4-dimethoxy phenylhydrazine hydrochloride in a mixture of 750 mls of ethanol, 750 mls of water and 350 mls of 5% hydrochloric acid. It is heated under a reflux, and then one adds over a period of 5 minutes a solution of 63 g of 1-(4,4-diethoxybutyl)-2-piperidone in 250 mls of ethanol. After heating under a reflux for 2 hours and then cooling, one eliminates the ethanol by distillation under reduced pressure (20 mm of mercury) and then extracts successively with 500 mls, 300 mls and 200 mls of methylene chloride. The combined organic phases are washed with 500 mls of water and then 500 mls of a saturated solution of sodium bicarbonate, dried over magnesium sulphate and evaporated to dryness under reduced pressure (20 mm of mercury). The residue (58 g) is chromatographed over 1 kg of silica gel contained in a column with a diameter of 6 cm, collecting fractions of 500 mls and eluting with ethyl acetate containing 1.5% of methanol. Fractions 31 to 43 are combined and evaporated to dryness. In this way one obtains 17 g of 1-[2(5,6-dimethoxy-3-indolyl) ethyl]-2-piperidone in the form of a thick yellow oil which slowly crystallises.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04138489
Source datasetuspto-grants-1979_02
ORD IDord-1ff8c84fbe634075b672b52334a34adb
Source noteuspto-grants-1979_02