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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043113Generated: October 29, 2026

6-Chloroquinoline → 6-Chloro-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/2043113

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-ChloroquinolineHCID 69163—
CatalystAdams' catalystHCID 345198—
SolventMethanolHCID 887—
Product6-Chloro-1,2,3,4-tetrahydroquinolineHCID 1118283962.7%

Reaction Steps

A flask filled with a mixture of 6-chloroquinoline (12.0 g, 73.3 mmol), PtO2 (2.16 g, 13 mol %), and MeOH (500 mL, 6.15 M) was flushed with N2 and then equipped with a balloon filled with H2. The reaction was kept under H2 atmosphere and stirred for 4 h. The mixture was filtered through Celite and washed with CH2Cl2. Purification via silica gel chromatography using 50% CH2Cl2 in hexanes gave 6-chloro-1,2,3,4-tetrahydroquinoline (7.7 g, 62%). 1H NMR (400 MHz, DMSO-d6) δ 6.85-6.83 (m, 2H), 6.42-6.39 (m, 1H), 5.82 (s, 1H), 3.17-3.13 (m, 2H), 2.64 (t, J=6.3 Hz, 2H), 1.78-1.72 (m, 2H). LC/MS (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)), m/z: M+1 obs=168.2; tR=1.57 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586589B2
Source datasetuspto-grants-2013_11
ORD IDord-6f98c39ca3b34e60b94b9b937d66faa1
Source noteuspto-grants-2013_11