HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336868Generated: October 25, 2026
Water → Ethyl 4-(4-benzylphenylamino)-6-chloroquinoline-3-carboxylate
https://huagongshe.com/reaction/336868
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Benzenamine, 4-(phenylmethyl)- | HCID 136914 | — |
| Reactant | Ethyl 4,6-dichloroquinoline-3-carboxylate | HCID 1479087 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ethyl 4-(4-benzylphenylamino)-6-chloroquinoline-3-carboxylate | HCID 58524965 | 71.3% |
Reaction Steps
To a solution of Ethyl-4,6-dichloroquinoline-3-carboxylate (1.0 g, 3.7 mmol) in 1,4-dioxane (10 mL) was added a solution of 4-benzylbenzenamine (733 mg, 4.0 mmol) in 1,4-dioxane (10 mL) at room temperature. After stirred at 85° C. 1 hour, the reaction mixture was then cooled down to room temperature and then treated with 20 mL of water. The resulting suspension treated with 10 NNaOH solutions to reach the pH about 9. It was partitioned between ethyl acetate and water. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over MgSO4, filtered and concentrated. The crude product was purified by flash column chromatography using a 9:1 v/v hexane:ethyl acetate as solvent to afford title compound (1.1 g, 65% yield) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889706B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-076b882cf409432d86bd7f4ecf398f0e |
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| Source note | uspto-grants-2014_11 |
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