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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451165Generated: October 31, 2026

Oxalyl chloride → HCID 19966727, compound

https://huagongshe.com/reaction/1451165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2-(1H-Pyrrol-1-yl)isoindoline-1,3-dioneHCID 853719—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 19966727HCID 19966727—

Reaction Steps

A suspension of anhydrous aluminium chloride (3.1 g; 4.7×5 mM) in 20 ml of 1,2-dichloroethane was cooled with ice to 0°-5° C., and oxalyl chloride (3 g; 4.7×5 mM) was added dropwise to the suspension. After stirred at 0°-5° C. for 20 minutes, a suspension of N-(1H-pyrrol-1-yl)phthalimide (IX-I; 1.0 g; 4.7 mM) in 1,2-dichloroethane was added thereto. Thereafter, the mixture was stirred for 50 minutes with slowly raising the temperature to room temperature. The reaction mixture was poured into ice water and insoluble materials was removed by filteration. To the filtrate was added ethyl acetate with thoroughly stirring to separate an organic phase. The organic phase was dried with sodium sulfate, and the solvent was then removed by distillation to obtain the compound (IX-61)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05604178
Source datasetuspto-grants-1997_02
ORD IDord-a17717f6d2c243d39b3779caf51ce7fc
Source noteuspto-grants-1997_02