HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010076Generated: October 29, 2026
Ethanol → 4-(4-Aminophenoxy)-7-(benzyloxy)-6-cyanoquinoline
https://huagongshe.com/reaction/1010076
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 7-Benzyloxy-6-cyano-4-(4-nitrophenoxy)quinoline | HCID 22936590 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(4-Aminophenoxy)-7-(benzyloxy)-6-cyanoquinoline | HCID 22936831 | — |
Reaction Steps
Iron powder (0.6 g), ammonium chloride (1.4 g), ethanol (100 ml) and water (30 ml) were added to the 7-benzyloxy-6-cyano-4-(4-nitrophenoxy)quinoline obtained in Production Example 5, and the mixture was stirred at 90° C. for 2.5 hours. The reaction system was returned to room temperature and then filtered with celite, the filtrate was subjected to liquid separation, and the organic layer was washed with water and saturated brine in that order, dried over sodium sulfate and then concentrated to dryness under reduced pressure to obtain 1.31 g of a crude product containing the target substance. The crude product was used directly for the following reaction. (Production Example 7).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07973160B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-d0f79b4c20d04e999a1c61eeb1e4838b |
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| Source note | uspto-grants-2011_07 |
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