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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844392Generated: November 1, 2026

Ethyl acetate hexane → HCID 136241951, compound

https://huagongshe.com/reaction/1844392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl acetate hexaneHCID 21226206—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 86727907HCID 86727907—
SolventTetrahydrofuranHCID 8028—
ProductHCID 136241951HCID 136241951—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(Phenylethynyl)quinoline-5-ylpivalate (15.4 mg, 0.0468 mmol) was dissolved in THF (0.78 mL), followed by cooling down to 0° C. After LiAlH4 (0.06 mL, 0.117 mmol) was added thereto, the resulting mixture was warmed to room temperature and stirred for 1 hr. The completion of the reaction was confirmed by TLC (EtOAc/Hexane=1:1). When the reaction was completed, a saturated aqueous solution was added thereto, and the resulting mixture was extracted with diethylether, to thereby obtain an organic layer. The organic layer was dried over anhydrous MgSO4 and filtrated. The filtrate was concentrated under reduced pressure and purified by column chromatography (EtOAc/Hexane=1:1, R.f: 0.7), to thereby obtain 2-(phenylethynyl)quinoline-5-ol (5.6 mg, 49%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946431B2
Source datasetuspto-grants-2015_02
ORD IDord-07bb8e9631e04f5a9e3ef28c8aacfda7
Source noteuspto-grants-2015_02