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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378377Generated: October 29, 2026

Ammonium Chloride → 1-[1-(1-Methylethyl)-1,2,3,4-tetrahydroquinolin-6-yl]ethanol

https://huagongshe.com/reaction/378377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Isopropyl-1,2,3,4-tetrahydro-quinoline-6-carbaldehydeHCID 3157489—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
Product1-[1-(1-Methylethyl)-1,2,3,4-tetrahydroquinolin-6-yl]ethanolHCID 10608918—

Reaction Steps

4.9 ml (15 mmol) of a 3.0M ethereal solution of methylmagnesium bromide was diluted with 15 ml of ether. An ethereal solution of 2.0 g (10 mmol) of 1-(1-methylethyl)-1,2,3,4-tetrahydroquinoline-6-carbaldehyde was dropped into the dilution prepared above at room temperature. The obtained mixture was stirred at room temperature for one hour, followed by the addition of an aqueous solution of ammonium chloride. The resulting mixture was extracted with thyl acetate. The organic phase was washed with a saturated aqueous solution of common salt, dried over anhydrous magnesium sulfate and concentrated in a vacuum to give 2.1 g of the title compound as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030964
Source datasetuspto-grants-2000_02
ORD IDord-5fd77841b5e0440790f62b049f953a51
Source noteuspto-grants-2000_02