HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833194Generated: November 2, 2026
1,3-Dibromopropane → HCID 22048409, compound
https://huagongshe.com/reaction/1833194
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,3-Dibromopropane | HCID 8001 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 135714882 | HCID 135714882 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22048409 | HCID 22048409 | 63.6% |
Reaction Steps
To a stirred solution of 6-hydroxy-7-methoxy-1-(3-ethoxy-benzyl)-isoquinoline-4-carbaldehyde (86 g, 0.24 mmol) in N,N-dimethylformamide (2 mL) was added potassium carbonate (337 mg, 2.40 mmol) and 1,3-dibromopropane (0.124 mL, 1.22 mmol) at room temperature. The reaction mixture was heated 85° C. for 2 hrs. The solvent was evaporated and the residue was purified on a flash chromatography (Merck Silica gel 60, 70–230 mesh, 50% ethyl acetate/hexane) to afford product 6-(3-bromo-propoxy)-7-methoxy-1-(3-ethoxy-benzyl)-isoquinoline-4-carbaldehyde as a colorless oil (70 mg, 62% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07067529B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-424afefd790e46529523db5fe3dacd9d |
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| Source note | uspto-grants-2006_06 |
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