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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53219Generated: October 30, 2026

Potassium Sodium Tartrate → 3-Quinolinepropanol

https://huagongshe.com/reaction/53219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Sodium TartrateHCID 9357—
ReactantEthyl 3-quinolinepropionateHCID 14338577—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
Product3-QuinolinepropanolHCID 1908202185%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.) solution of ethyl 3-(3quinolyl)propionate (1.01 g, 4.4 mmol) in 20 ml of ether was added 2.6 ml (2.6 mmol) of 1M LAH solution at 0° C. After stirring at 0° C. for 15 min, the mixture was allowed to warm and stirred at 20° C. for 3 h, and Rochelle salt (equiv) was added. The mixture was extracted with methylene chloride, and the organic layer was dried over sodium sulfate, and concentrated in vacuo. The residue was purified by chromatography on silica (10 cm column, ethyl acetete/hexane, 1/2-5/1; methylene chloride/acetone, 2/1-1/4) to afford 700 mg (85%) of 3-(3-hydroxypropyl)quinoline, as a thick oil. 3-[3-[4-(5-Trifluoromethyl-1,2,4-oxadiazol-3-yl)-2,6-dimethylphenoxy]-propyl]-quinoline (I, Q=3-quinolyl Y=1,3-propylene, R1,R2 =3,5-dimethyl, R3 =5-trifluoromethyl-1,2,4-oxadiazol-3-yl)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05618821
Source datasetuspto-grants-1997_04
ORD IDord-79ea1e225a8f47aa9a9333017b9afbdf
Source noteuspto-grants-1997_04