HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68533Generated: October 28, 2026
HCID 86696916, compound → 7-(3-Chloropropoxy)-6-methoxyquinolin-4-OL
https://huagongshe.com/reaction/68533
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86696916 | HCID 86696916 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 7-(3-Chloropropoxy)-6-methoxyquinolin-4-OL | HCID 71744012 | 67.1% |
Reaction Steps
Intermediate IV (150 g, 0.44 mol) was added to glacial acetic acid (8v/w, 1200 mL). The mixture was warmed up to 40° C. After Intermediate IV was dissolved completely, iron powder (123.1 g, 2.20 mol) was slowly added in batch. The mixture was warmed up to 80° C. and reacted under mechanical stirring for 2 h. After completion of the reaction, the reaction solution was filtered by suction when it is still hot. The filtrate was collected. After cooling the filtrate, a great deal of solid separated out and was filtered by suction to produce a lutescens solid. The filtered cake was dissolved in glacial acetic acid. The mixture was stirred at 80° C. for about 30 min, and was filtered by suction again when it is still hot. The filtrate was collected. After cooling the filtrate, a solid separated out and was filtered by suction to produce a lutescens solid. The solids were combined, and washed with water several times until the filtrate became neutral. The filtered cake was dried to produce a pale yellow solid (79 g) in a yield of 65%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822465B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-ce660921652a4a569557cd90a8f6ce41 |
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| Source note | uspto-grants-2014_09 |
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