Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244083Generated: October 25, 2026

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

https://huagongshe.com/reaction/244083

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 rt 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 numberUS08653268B2
Source datasetuspto-grants-2014_02
ORD IDord-f3194c22ba01430a93a11aaa354a6fc3
Source noteuspto-grants-2014_02