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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902195Generated: October 26, 2026

Acetic Anhydride → Ethyl 3-acetyl-4,5-dimethyl-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/902195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl 4,5-dimethyl-1H-pyrrole-2-carboxylateHCID 137478—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,1-DichloroethaneHCID 6365—
ProductEthyl 3-acetyl-4,5-dimethyl-1H-pyrrole-2-carboxylateHCID 1228839960%

Reaction Steps

To a solution of aluminum chloride (50.19 g, 0.376 mol) in dry dichloroethane (580 mL) at 25° C. was added slowly acetic anhydride (17.75 mL, 0.188 mol). The resulting mixture was stirred at room temp. for 10 minutes, then a solution of pyrrole 33 (10.49 g, 0.0627 mol) in dichloroethane (30 mL) was added and the reaction mixture was stirred at room temp. for 2 h. After an additional 3 h at 80° C., the mixture was poured into ice water and extracted with dichloromethane. The organic layer was dried with anhy. sodium sulfate and concentrated in vacuo to an orange residue. Short plug filtration over silica gel (30% ethyl acetate/70% hexanes) gave 7.5 g (60%) of ethyl-3-acetyl-4,5-dimethyl-2-pyrrole carboxylate 34. 1H NMR (CDCl3) d 9.0 (bs,1H), 4.3 (q,2H), 2.7 (s,3H), 2.1 (s, 3H), 1.9 (s,3H), 1.3 (t,3H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365092B2
Source datasetuspto-grants-2008_04
ORD IDord-f7d102a0133049ad99cacba55de6f0b2
Source noteuspto-grants-2008_04