Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763169Generated: November 1, 2026

Acetic Anhydride → HCID 54074224, compound

https://huagongshe.com/reaction/1763169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTetrachlorophthalic anhydrideHCID 8326—
ReactantSodium HydroxideHCID 14798—
Reactant4-[1-(4-Ethoxyphenyl)ethenyl]-N,N-dimethylanilineHCID 14512255—
SolventWaterHCID 962—
Solvent1,2-DichlorobenzeneHCID 7239—
ProductHCID 54074224HCID 5407422480.8%

Reaction Conditions

Temperature120 °C

Reaction Steps

Into a mixture of 25 ml of acetic anhydride and 75 ml of o-dichlorobenzene, 13.4 g of 1-(p-ethoxyphenyl)-1-(p-dimethylaminophenyl)ethylene (melting at 110°-111° C.) and 21.5 g of tetrachlorophthalic anhydride were added and the mixture was stirred for 6 hours at 120° C. After adding the reaction mixture into 200 ml of water and making the mixture alkaline by sodium hydroxide, the alkaline mixture was extracted with 70 ml of toluene. The solid matter obtained by distilling off toluene from the extract was recrystallized from acetone while purifying with activated carbon to obtain 16.2 g of pale yellow crystals in a yield of 80.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04835291
Source datasetuspto-grants-1989_05
ORD IDord-ec5b4c14384a4b7198296d0079296fdd
Source noteuspto-grants-1989_05