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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814300Generated: November 3, 2026

Methanol → 2-(Quinolin-5-yl)ethan-1-ol

https://huagongshe.com/reaction/1814300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
ReactantSodium borohydrideHCID 4311764—
Reactant5-(2-Propen-1-yl)quinolineHCID 22504110—
Product2-(Quinolin-5-yl)ethan-1-olHCID 2250413250%

Reaction Steps

5-Allyl-quinoline (3.12 g, 18.4 mmol) was dissolved in 40 mL methanol and 40 mL methylene chloride and cooled to −78° C. Ozone was bubbled in until a green solution was seen. Sodium borohydride (1.4 g, 36.8 mmol) was added. The reaction was warmed to room temperature and stirred for 2 hours. The reaction was quenched with water. A saturated solution of KHPO4 was added and the mixture extracted with methylene chloride. The organic extracts were dried with Na2SO4, filtered, and concentrated in vacuo. The crude product was chromatographed with ethyl acetate to yield 1.6 g (50%) of 2-quinolin-5-yl-ethanol as a yellow solid. MS (APCI) m/z 174.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875765B2
Source datasetuspto-grants-2005_04
ORD IDord-49d5dbc8d34b426d8bfb9fe3cb872e4b
Source noteuspto-grants-2005_04