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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493122Generated: November 2, 2026

Toluene → HCID 68982683, compound

https://huagongshe.com/reaction/493122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantDiethyl CarbonateHCID 7766—
ReactantSodium amideHCID 24533—
Reactant6-Methoxy-4-methylquinolineHCID 258761—
SolventDiethyl EtherHCID 3283—
ProductHCID 68982683HCID 6898268316%

Reaction Conditions

Temperature0 °C

Reaction Steps

6-Methoxy-4-methyl-quinoline (0.791 g, 4.572 mmol) was dissolved in anhydrous diethyl ether and cooled to 0° C. under an argon atmosphere. To the stirred mixture was added sodamide as a 50% w/w slurry in toluene (0.36 g, 4.57 mmol). The resulting slurry was allowed to warm to room temperature and was stirred for 1 hour. To this was added diethylcarbonate (0.28 ml, 2.29 mmol). The reaction mixture was then stirred at reflux for 10 hours after which time it was quenched with water (2 ml). The mixture was partitioned between ethyl acetate (2×100 ml) and water (20 ml). The organic phases were combined and dried over magnesium sulfate. The volatiles were removed under reduced pressure and the residue subjected to purification on silica gel using an ethyl acetate-hexane gradient. This provided the desired product as a brown oil (90 mg, 7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534793B2
Source datasetuspto-grants-2009_05
ORD IDord-10226567c01b46eab0db92d1dc608a27
Source noteuspto-grants-2009_05