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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852249Generated: October 25, 2026

Phosphorus oxychloride → 3-(4-(Tert-butyl)phenyl)-1-chloro-6-methoxyisoquinoline

https://huagongshe.com/reaction/1852249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant3-(4-(tert-butyl)phenyl)-6-methoxyisoquinolin-1(2H)-oneHCID 70979018—
Product3-(4-(Tert-butyl)phenyl)-1-chloro-6-methoxyisoquinolineHCID 8668326928%

Reaction Steps

A solution of 3-(4-(tert-butyl)phenyl)-6-methoxyisoquinolin-1(2H)-one (0.7 g, 2.277 mmol) in POCl3 (7 ml) was refluxed for overnight. The solvent was evaporated under reduced pressure and the residue was diluted with cold water. The aqueous solution was basified by solid sodium carbonate and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure to get crude compound. The crude compound was purified by silica gel chromatography (10% ethyl acetate in pet ether) to get desired compound (0.21 g, 28.0%) as solid. 1H NMR (400 MHz, DMSO-d6): δ ppm 8.34(s, 1H), 8.18-8.16 (d, J=8 Hz, 1H), 8.08-8.06 (d, J=8 Hz, 2H), 7.57-7.55 (d, J=8 Hz, 2H), 7.41 (s, 1H), 7.40-7.38 (d, J=8 Hz, 1H), 3.97 (s, 3H), 1.34 (s, 9H); MS: MS m/z 362.2 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957203B2
Source datasetuspto-grants-2015_02
ORD IDord-c0a156650a184eb2bbb2c3f68ed63fbc
Source noteuspto-grants-2015_02