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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514652Generated: November 2, 2026

Acetyl chloride → HCID 66670262, compound

https://huagongshe.com/reaction/1514652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantSodium HydroxideHCID 14798—
ReactantTin tetrachlorideHCID 24287—
ReactantHCID 66670203HCID 66670203—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 66670262HCID 66670262—

Reaction Steps

Bioorganic & Medicinal Chem. Lett., 14 (2004), 1295-1298, was used as a reference. A 1.00 g portion of ethyl 5-tert-butyl-1-[2-(4-fluorophenyl)ethyl]-2-methyl-1H-pyrrole-3-carboxylate was dissolved in 15 ml of toluene, 0.26 ml of acetyl chloride was added thereto, and 3.6 ml of tin(IV) chloride (a 1 M dichloromethane solution) was added dropwise thereto at 0° C., followed by stirring at room temperature for 6 hours. After adjusting to pH 12 by adding 25 ml of a 1 M sodium hydroxide aqueous solution at 0° C., extraction was carried out with ethyl acetate, followed by washing with saturated brine. After drying with anhydrous sodium sulfate, the solvent was evaporated under a reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:10-1:7-1:5) to obtain 668 mg of ethyl 5-acetyl-1-[2-(4-fluorophenyl)ethyl]-2-methyl-1H-pyrrole-3-carboxylate as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222274B2
Source datasetuspto-grants-2012_07
ORD IDord-b435ecac0bbe47b5a0f369c00353389c
Source noteuspto-grants-2012_07