HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537180Generated: October 30, 2026
Sodium Methoxide → 7-Bromo-3-methoxyisoquinoline
https://huagongshe.com/reaction/537180
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 7-Bromo-3-chloroisoquinoline | HCID 51341980 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | 7-Bromo-3-methoxyisoquinoline | HCID 67491766 | 87.2% |
Reaction Steps
A mixture of 7-bromo-3-chloroisoquinoline (100 mg, 0.4 mmol) and sodium methoxide (113 mg, 2.1 mmol) in diglyme (1 mL) was heated to 150° C. for 1 hour. The reaction was cooled to room temperature and diluted with toluene and water. The layers were separated and the aqueous layer was extracted with toluene (3×). The combined organics were washed with water and brine, dried over sodium sulfate, filtered, and concentrated to an oil. The oil was dried under vacuum overnight to give the title compound (83 mg, 85%) as a yellow solid. +ESI (M+H+1) 240.1; 1H NMR (400 MHz, CDCl3, δ): 8.87 (s, 1H), 8.01-8.05 (m, 1H), 7.58-7.64 (m, 1H), 7.53-7.58 (m, 1H), 6.97 (s, 1H), 4.02 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859773B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-8c9004d58bcf45a4ba165d8dd68d2144 |
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| Source note | uspto-grants-2014_10 |
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