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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531383Generated: October 30, 2026

Quinoline → 2-Amino-4-hydroxy-3-methylbenzonitrile

https://huagongshe.com/reaction/531383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinolineHCID 7047—
ReactantSodium HydroxideHCID 14798—
ReactantN-(hept-6-enyl)phthalimideHCID 53236045—
Product2-Amino-4-hydroxy-3-methylbenzonitrileHCID 1346471682%

Reaction Conditions

Temperature170 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353103B2
Source datasetuspto-grants-2016_05
ORD IDord-c9a0e766973a40a0a07e0d9f7feb87c4
Source noteuspto-grants-2016_05