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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantAmmonium ChlorideHCID 25517—
Reactant7-Benzyloxy-6-cyano-4-(4-nitrophenoxy)quinolineHCID 22936590—
CatalystIronHCID 23925—
SolventWaterHCID 962—
Product4-(4-Aminophenoxy)-7-(benzyloxy)-6-cyanoquinolineHCID 22936831—

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973160B2
Source datasetuspto-grants-2011_07
ORD IDord-d0f79b4c20d04e999a1c61eeb1e4838b
Source noteuspto-grants-2011_07