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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432853Generated: November 1, 2026

Water → 7-Chloro-3-methylisoquinoline

https://huagongshe.com/reaction/1432853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
ReactantSodium HydroxideHCID 14798—
Reactant1,7-Dichloro-3-methylisoquinolineHCID 21388033—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product7-Chloro-3-methylisoquinolineHCID 20616795—

Reaction Steps

To a solution of 1,7-dichloro-3-methyl-isoquinoline (0.50 g, 2.36 mmol), Example 10, part C, in 5.5 mL of 9:1 acetic acid:H2O at 75° C. is added zinc (0.23 g, 3.54 mmol) After 75 minutes, the solution is cooled to ambient temperatures. The solution is diluted with a 4:1 EtOAc:CH2Cl2 solution. To the solution is added 100 mL of a 1N NaOH solution. The aqueous solution is extracted with 4:1 EtOAc:CH2Cl2. The combined organic layers are washed with a saturated NaCl solution. The organic layer is dried over MgSO4, filtered and concentrated. The crude product is purified by column chromatography eluting with a gradient of 5% EtOAc/hexanes to 15% EtOAc/hexanes. The title compound is obtained as a white solid (0.36 g, 1.97 mmol). 1H NMR (CDCl3, 300 MHz) δ9.09 (s, 1H), 7.89 (s, 1H), 7.61 (d, 1H), 7.55 (d, 1H), 7.44 (s, 1H) 2.68 (s, 3H). MS (EI): m/z 177, 179 (M+), Cl pattern.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612075B2
Source datasetuspto-grants-2009_11
ORD IDord-595e036b8b124e528a56eb6c6c912ffc
Source noteuspto-grants-2009_11