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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028692Generated: October 31, 2026

2-Phenylquinoline-7-carboxylic acid hydrochloride → (2-Phenylquinolin-7-yl)methanol

https://huagongshe.com/reaction/1028692

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Phenylquinoline-7-carboxylic acid hydrochlorideHCID 15946870—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(2-Phenylquinolin-7-yl)methanolHCID 22062823—

Reaction Steps

Under N2, to a solution of 2-phenylquinoline-7-carboxylic acid hydrochloride (144 mg, 0.5 mmol) in THF (5 mL) was added LiAlH4 (95 mg, 2.5 mmol) in two portions. The mixture was stirred at it for 15 h, quenched with water (1 mL), and filtered through a Celite pad, which was washed with EtOAc (30 mL). The combined filtrates were dried over MgSO4, filtered, concentrated, and purified by silica gel chromatography (5% MeOH in dichloromethane) to afford the desired product. 1H-NMR (CDCl3, 400 MHz) δ 4.93 (s, 2H), 7.46-7.57 (m, 4H), 7.84 (d, J=8.4 Hz, 1H), 7.88 (d, J=8.8 Hz, 1H), 8.14-8.18 (m, 3H), 8.23 (d, J=8.4 Hz, 1H). MS (ES+): m/z 236 [MH+]. HPLC: tR=2.72 min (OpenLynx, polar—5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735405B2
Source datasetuspto-grants-2014_05
ORD IDord-b1903a3e515d4fc7ac99a8471b83b35d
Source noteuspto-grants-2014_05