HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913124Generated: October 31, 2026
Benzyl Bromide → 1-Benzyloxy-7-chloro-6-fluoro-isoquinoline
https://huagongshe.com/reaction/1913124
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 7-Chloro-6-fluoroisoquinolin-1(2H)-one | HCID 59818248 | — |
| Catalyst | HCID 178418647 | HCID 178418647 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-Benzyloxy-7-chloro-6-fluoro-isoquinoline | HCID 59818252 | 54.2% |
Reaction Steps
14.74 g (74.6 mmol) of 7-chloro-6-fluoro-2H-isoquinolin-1-one (101) were dissolved in 150 ml of toluene. After addition of 30.86 g (111.9 mmol) of silver carbonate and 15.31 g (89.5 mmol) of benzyl bromide, the mixture was stirred at 80° C. for 3 h. After cooling down to room temperature, the reaction mixture was filtered and the filtrate was evaporated. The residue was dissolved in dichloromethane and washed with water, dried with magnesium sulfate and evaporated. Final purification by preparative HPLC gave 11.63 g of the title compound. Rt=2.51 min (Method B). Detected mass: 288.1/290.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08609691B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-da9b4eaa363a4de7917dfc8b6cee24f9 |
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| Source note | uspto-grants-2013_12 |
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