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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451976Generated: October 25, 2026

Acetyl chloride → 2-(2-Acetyl-1H-pyrrol-1-yl)-1H-isoindole-1,3(2H)dione

https://huagongshe.com/reaction/1451976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTin tetrachlorideHCID 24287—
Reactant2-(1H-Pyrrol-1-yl)isoindoline-1,3-dioneHCID 853719—
SolventDichloromethaneHCID 6344—
Product2-(2-Acetyl-1H-pyrrol-1-yl)-1H-isoindole-1,3(2H)dioneHCID 19966752—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of acetyl chloride (6.77 ml) in DCM (400 ml) was added tin (IV) chloride (11.14 ml) at -5° C., under nitrogen. 2-(1H-pyrrol-1-yl)-1H-isoindole-1,3(2H)dione (20.0 g) was then added portion-wise, keeping the temperature below 0° C. The reaction mixture was then stirred at 0° C. for 0.5 hour, at which time it was poured into ice water. The layers were separated and the aqueous phase was extracted with DCM. The combined organics were washed twice with 5% HCl (aq.) and dried (MgSO4). Filtration and concentration gave the etude product. Purification via flash column chromatography (silica gel, DCM) afforded 9.62 g of the product as a solid, m.p. 204°-205° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05605925
Source datasetuspto-grants-1997_02
ORD IDord-3657eebc9e4441f093c1d8d583236da9
Source noteuspto-grants-1997_02