HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963982Generated: October 27, 2026
Isoquinolin-5-ol → 2-[4,4-Bis-(4-fluorophenyl)butyl]-5-hydroxyisoquinolinium bromide
https://huagongshe.com/reaction/963982
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isoquinolin-5-ol | HCID 30386 | — |
| Reactant | 1,1'-(4-Bromobutylidene)bis[4-fluorobenzene] | HCID 93763 | — |
| Product | 2-[4,4-Bis-(4-fluorophenyl)butyl]-5-hydroxyisoquinolinium bromide | HCID 15870891 | — |
Reaction Steps
A mixture of 5-hydroxyisoquinoline (4.56 g, 31.41 mmol) and 4,4-bis(4-fluorophenyl)butyl bromide (11.40 g, 35.06 mmol. Prepared according to the procedure of Miroslav Rajsner, et al., Czech. Collect. Czech. Chem. Commun., 1978;43:1760) in 100 mL of anhydrous DMF was stirred at 80° C. overnight. The reaction mixture was cooled to 0° C. Ethyl acetate (400 mL) was added to precipitate product. The solid was collected by filtration and washed with ethyl acetate (2×100 mL). The solid was air-dried to give 10.74 g of product as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05767129 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-709147a52d124a7b9b8ef1ecf1ac8405 |
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| Source note | uspto-grants-1998_06 |
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