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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355578Generated: November 4, 2026

5-Nonanone → HCID 9844775, compound

https://huagongshe.com/reaction/1355578

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-NonanoneHCID 10405—
ReactantHCID 69876357HCID 69876357—
SolventIsopropanolHCID 3776—
ProductHCID 9844775HCID 98447759.3%

Reaction Steps

To a solution of (1R)-1-(4,5-dimethyl-1,3-oxazol-2-yl)-2-(1H-indol-3-yl)-1-ethanamine hydrochloride (1.2 g, 3.6 mmol) in isopropanol (20 ml) was added 5-nonanone (3.1 ml, 20 mmol) and the mixture was refluxed for about 24 hours. The solvent was evaporated under reduced pressure. To the residue was added water (20 ml) followed by NaHCO3 (10%) solution until neutral pH, followed by ethyl acetate (3×15 ml). After decantation and extraction the combined organic extracts were washed with water (20 ml) and dried over MgSO4. The solvent was evaporated under reduced pressure to afford an oil which was purified by column chromatography on silica gel using ethyl acetate/heptane 7:3 as eluent. The resulting oil was dissolved in ethyl acetate (15 ml) and a solution of HCl in ethyl acetate (1N) was slowly added at about 20° C. to give a precipitate. The suspension was stirred a few minutes and the precipitate collected by filtration, washed with diethyl ether, and dried to afford 0.14 g the desired product as the hydrochloride salt. Melting point: 128-134° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586445B1
Source datasetuspto-grants-2003_07
ORD IDord-0188ef1d8d684e1084ea89d7d5d9937b
Source noteuspto-grants-2003_07