HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277382Generated: October 31, 2026
4-Nitrophenol → 7-(Benzyloxy)-4-(4-nitrophenoxy)quinoline
https://huagongshe.com/reaction/2277382
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 7-(Benzyloxy)-4-chloroquinoline | HCID 22030657 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-(Benzyloxy)-4-(4-nitrophenoxy)quinoline | HCID 68193942 | 95.7% |
Reaction Steps
To a suspension of 7-(benzyloxy)-4-chloroquinoline (10 g, 37.1 mmol) and 4-nitrophenol (6.2 g, 44.5 mmol) in toluene (10 mL) was added DIPEA (6.2 g, 48.2 mmol). The reaction mixture was refluxed at 115° C. for 12 hours, then cooled down to room temperature. DCM (50 mL) was added to the mixture, and the resulted solution was washed with 1 M NaOH (30 mL each) several times till the water phase was colorless. The organic phase was concentrated in vacuo to afford a brown solid (13.2 g, 95.7%). The solid was stirred in 95% EtOH (30 mL) at room temperature for 12 hours, and filtered to give the title compound as a gray-brown solid (12.1 g, 91.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133162B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-ad6b578ce7bb451393ef739e4e7c9944 |
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| Source note | uspto-grants-2015_09 |
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