Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259857Generated: October 31, 2026

Thionyl Chloride → HCID 22403871, compound

https://huagongshe.com/reaction/259857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 22403924HCID 22403924—
CatalystDimethylformamideHCID 6228—
ProductHCID 22403871HCID 22403871—

Reaction Steps

A mixture of 4-acetoxy-3,5-diisopropylbenzoic acid (634 mg), thionyl chloride (3 ml) and DMF (1 drop) was refluxed for 40 minutes, concentrated and evaporated to obtain 4-acetoxy-3,5-diisopropylbenzoyl chloride. The resultant was dissolved in dichloromethane (20 ml), to which 3-amino-4-(2-chlorophenyl)-6,8-dimethylquinoline (566 mg) and triethylamine (0.30 ml) were added. Thus obtained solution was stirred at room temperature for one night. After dilution with water, the solution was extracted with dichloromethane. The dichloromethane layer was washed with 2N-hydrochloric acid and water, and then dried (MgSO4). The solvent was removed and the residue was recrystallized from ethanol to obtain 3-(4-acetoxy-3,5-diisopropylbenzamido)-4-(2-chlorophenyl)-6,8-dimethylquinoline (815 mg, 77.0%) as colorless prisms.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05523407
Source datasetuspto-grants-1996_06
ORD IDord-bb80ec533bd543a19e73ef7050dd4e93
Source noteuspto-grants-1996_06