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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Reactant | 2-(1H-Pyrrol-1-yl)isoindoline-1,3-dione | HCID 853719 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(2-Acetyl-1H-pyrrol-1-yl)-1H-isoindole-1,3(2H)dione | HCID 19966752 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05605925 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-3657eebc9e4441f093c1d8d583236da9 |
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| Source note | uspto-grants-1997_02 |
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