Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430405Generated: November 1, 2026

Toluene → HCID 67954048, compound

https://huagongshe.com/reaction/1430405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantIodoethaneHCID 6340—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 67953980HCID 67953980—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
ProductHCID 67954048HCID 67954048—

Reaction Conditions

Temperature45 °C

Reaction Steps

8-benzyloxy-1-methyl-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione (33.4 g, 113 mmol), tetrabutyl ammonium bromide (7.28 g, 22.6 mmol) and an aqueous solution of 25% sodium hydroxide (20.8 g, 130 mmol) were added to the mixture of toluene (167 mL) and water (150 mL). Ethyl iodide (10.4 mL, 130 mmol) was added thereto, and the reaction was performed at 80° C. for 4 hours. The reaction solution was cooled, and ethyl acetate (334 mL) extraction was performed. The resulting organic layer was washed with water, and the solvent was distilled off under reduced pressure. Ethyl acetate (70 mL) was added to the resulting residue, and the mixture was heated and dissolved. Thereafter, hexane (35 mL) was added thereto, and heating was performed again. The mixture was stirred at 40-50° C. for 30 minutes, and stirred under ice cooling for 1 hour to collect precipitated crystals by filtration. The resulting crystals were washed with ethyl acetate-hexane (1:1; 50 mL), and dried at 60° C., thereby obtaining 39.6 g of a light-yellow, powdery target compound (containing ammonium salt).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940889B2
Source datasetuspto-grants-2015_01
ORD IDord-b54b5fded83c4c9abb9e98986cc18a65
Source noteuspto-grants-2015_01