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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282330Generated: November 1, 2026

Hydrochloric Acid → Methyl [5-(4-methoxybenzoyl)-1-methyl-1H-pyrrol-2-yl]acetate

https://huagongshe.com/reaction/1282330

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactantp-Anisoyl chlorideHCID 7477—
ReactantMethyl 1-methylpyrrol-2-acetateHCID 103992—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
ProductMethyl [5-(4-methoxybenzoyl)-1-methyl-1H-pyrrol-2-yl]acetateHCID 18424261—

Reaction Steps

A solution of 17.0 g. (0.1 mole) of p-anisoyl chloride and 13.3 g. (0.1 mole) of aluminum chloride in 200 ml. of methylene chloride is added over 5 minutes to a solution of methyl 1-methylpyrrole-2-acetate in 100 ml. of methylene chloride at ice bath temperature. The mixture is stirred for 25 minutes and poured into ice acidified with dilute hydrochloric acid. The organic layer is separated and the aqueous layer is washed with methylene chloride. The combined organic solutions are washed successively with dimethylaminopropylamine solution, dilute hydrochloric acid and brine and then dried over anhydrous magnesium sulfate. The solvent is evaporated in vacuo to give a dark oily residue which is crystallized from 40 ml. of cold methanol. The solid is collected by filtration, washed with cold methanol and recrystallized from methanol to give white crystalline methyl 5-(p-anisoyl)-1-methylpyrrole-2-acetate, m.p. 104-105° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455703B2
Source datasetuspto-grants-2002_09
ORD IDord-60ba5e7191634211ac3a30ce3a27df56
Source noteuspto-grants-2002_09