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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948732Generated: October 27, 2026

Ammonium Chloride → 1-(2-Chloro-8-methylquinolin-3-yl)ethanol

https://huagongshe.com/reaction/1948732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Chloro-8-methylquinoline-3-carboxaldehydeHCID 689082—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Chloro-8-methylquinolin-3-yl)ethanolHCID 2427607074.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a suspension of 2-chloro-8-methylquinoline-3-carboxaldehyde (10 g, 48.6 mmol) in dry THF (100 mL) under nitrogen cooled to −78° C. was added dropwise over 1 h methylmagnesium bromide (40 mL, 121.6 mmol, 3.0M solution in Et2O). The reaction was allowed to warm to r.t. and stirred for a further 1 h before being poured slowly into NH4Cl solution (100 mL). The mixture was extracted with EtOAc (2×200 mL) and the organic layers were combined, dried (MgSO4), filtered and concentrated in vacuo to afford the title compound as an off-white solid (8.0 g, 74%). δH (CDCl3) 8.33 (s, 1H), 7.68 (d, J 8.0 Hz, 1H), 7.55 (d, J 7.2 Hz, 1H), 7.44 (t, J 7.6 Hz, 1H), 5.34-5.40 (m, 1H), 2.77 (s, 3H), 1.61 (d, J 6.4 Hz, 3H). LCMS (ES+) 222, 224 (M+H)+, RT 3.01 minutes (Method 5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399483B2
Source datasetuspto-grants-2013_03
ORD IDord-d0346e2c9ab048e4880316a051996481
Source noteuspto-grants-2013_03