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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234751Generated: October 26, 2026

2-Chlorophenol → 2,5-Cyclohexadien-1-one, 2-chloro-4-((4-(diethylamino)-2-methylphenyl)imino)-

https://huagongshe.com/reaction/234751

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorophenolHCID 7245—
ReactantSodium CarbonateHCID 10340—
ReactantN,N-Diethyltoluene-2,5-diamine hydrochlorideHCID 108623—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2,5-Cyclohexadien-1-one, 2-chloro-4-((4-(diethylamino)-2-methylphenyl)imino)-HCID 10967590%

Reaction Conditions

Temperature55 °C

Reaction Steps

1450 parts K3Fe(CN)6, 595 parts Na2CO3, and 4150 parts water were added to a 12-liter round bottom flask equipped with a mechanical stirrer, thermometer, and addition funnel. The mixture was heated to 55° C. with stirring. A solution of 227 parts 4-(N,N-diethylamino)-2-methylaniline monohydrochloride, 128 parts o-chlorophenol, 1960 parts ethanol, and 2500 parts water was charged to the addition funnel and added dropwise to the stirred, heated solution. After the addition was complete the reaction mixture was maintained at 55° C. with stirring for 20 minutes. The warm mixture was filtered with vacuum and the resulting filter cake was placed in a solution of 296 parts ethanol and 1125 parts water to form a slurry. The dye was isolated by vacuum filtration. This process was repeated two times, first with 296 parts ethanol and 1125 parts water, then with 608 parts methanol. After the final vacuum filtration the filter cake was dried at 40° C. under vacuum for 48 hours. Yield was ~90%. The final product can be recrystallized from ethyl acetate or ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05596025
Source datasetuspto-grants-1997_01
ORD IDord-084edde874f649ec9ddd0f2e85d1e229
Source noteuspto-grants-1997_01