HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606140Generated: October 31, 2026
Hydrochloric Acid → Methyl [5-(4-methoxybenzoyl)-1-methyl-1H-pyrrol-2-yl]acetate
https://huagongshe.com/reaction/1606140
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | Methyl 1-methylpyrrol-2-acetate | HCID 103992 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl [5-(4-methoxybenzoyl)-1-methyl-1H-pyrrol-2-yl]acetate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03952012 |
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| Source dataset | uspto-grants-1976_04 |
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| ORD ID | ord-4d9f702c787b4d81896c6f6ff7884b92 |
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| Source note | uspto-grants-1976_04 |
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