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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982286Generated: November 1, 2026

1,2-Dichloroethane → HCID 20147792, compound

https://huagongshe.com/reaction/1982286

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-MethylpyrroleHCID 7304—
ReactantChlorobenzeneHCID 7964—
Reactant1(3H)-Isobenzofuranone, 6-(dimethylamino)-3-[4-(dimethylamino)phenyl]-HCID 93693—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventWaterHCID 962—
ProductHCID 20147792HCID 20147792—

Reaction Steps

To a stirred mixture of 75.0 ml of monochlorobenzene, 7.4 g of 3-(4-dimethylaminophenyl)-6-dimethylaminophthalide and 2.2 g of N-methylpyrrole maintained at 0°-5° C. by means of an external ice-bath, there was slowly added 6.65 g of anhydrous aluminum chloride. After stirring for approximately three hours, there was slowly added with continued cooling at 0°-5° C., 100 ml of water and 100 ml of ethylene dichloride. The layers were separated and the organic layer extracted with 150 ml of fresh water. The organic layer was then extracted with 100 ml of 3N hydrochloric acid, separated and the pH of this aqueous acid layer adjusted to 4.5 with five percent aqueous sodium hydroxide solution. The green solid which had formed was collected by filtration. After reslurrying in a mixture of acetone and methanol, the solid was filtered and dried to obtain 5.2 g of 2-[α-(4-dimethylaminophenyl)-α-(1-methyl-2-pyrrolyl)]methyl-5-dimethylaminobenzoic acid (Formula III: R=CH3 ; X=H; Y=4-(CH3)2 --NC6H4 ; Z=1-CH3 -2-pyrrolyl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04595768
Source datasetuspto-grants-1986_06
ORD IDord-2dad97f33d5e44f7ad13aad5b8239a55
Source noteuspto-grants-1986_06