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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257808Generated: November 1, 2026

Isopropanol → 1-Quinolin-6-ylcyclopropanecarbaldehyde

https://huagongshe.com/reaction/1257808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactant1-(Quinolin-6-yl)cyclopropanecarbonitrileHCID 66812840—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product1-Quinolin-6-ylcyclopropanecarbaldehydeHCID 59216277—

Reaction Conditions

Temperature-2.5 °C

Reaction Steps

Diisobutylaluminum hydride (1M in THF, 96 mL, 96 mmol) was added to a solution of 1-quinolin-6-ylcyclopropanecarbonitrile (12.4 g, 63.9 mmol) in toluene (120 mL) at −78° C. under an atmosphere of nitrogen. The reaction mixture was allowed to warm to −5 to 0° C., and stirred at that temperature for 3 h. The reaction mixture was cooled to −60° C. Isopropyl alcohol (10 mL) was carefully added dropwise. After stirring for 30 min, the reaction mixture was warmed to −5 to 0° C. The reaction mixture was diluted with ethyl acetate, quenched with water and extracted with ethyl acetate. The combined organic extracts were washed with water, brine, dried over sodium sulfate, filtered through a pad of silica gel eluting with 40% ethyl acetate in hexanes. The filtrate was concentrated to yield the desired product. (12 g, 95.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461330B2
Source datasetuspto-grants-2013_06
ORD IDord-ce3b2f4dfb364972b59643db8527eb72
Source noteuspto-grants-2013_06