HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402200Generated: October 29, 2026
Quinoline → 2-Amino-4-hydroxy-3-methylbenzonitrile
https://huagongshe.com/reaction/402200
Participants
| Role | Name | HCID | Charge |
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| Reactant | Quinoline | HCID 7047 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-(hept-6-enyl)phthalimide | HCID 53236045 | — |
| Product | 2-Amino-4-hydroxy-3-methylbenzonitrile | HCID 13464716 | 82% |
Reaction Steps
A mixture of compound 75 (19 g, 0.1 mol) in quinoline (50 mL) was heated to 170° C. for 2 h (until effervescence ceased). The reaction mixture was cooled to RT and aqueous NaOH solution was added (1M, 500 mL) followed by pet. ether (500 mL). The reaction mixture was stirred for 15 min and the aqueous layer was separated. The aqueous layer was further washed with pet. ether (2×300 mL) to remove quinoline completely. The aqueous layer was acidified with 1.5N HCl to pH=5, the solid was filtered off and dried under vacuum. The obtained solid was further washed with 5% ethyl acetate in pet. ether to give pure title compound (12 g, 82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741926B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-aa4ce2d37feb495aa6594d3515388459 |
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| Source note | uspto-grants-2014_06 |
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