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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 3-(4-(tert-butyl)phenyl)-6-methoxyisoquinolin-1(2H)-one | HCID 70979018 | — |
| Product | 3-(4-(Tert-butyl)phenyl)-1-chloro-6-methoxyisoquinoline | HCID 86683269 | 28% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957203B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-c0a156650a184eb2bbb2c3f68ed63fbc |
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| Source note | uspto-grants-2015_02 |
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