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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241714Generated: October 26, 2026

Methyl iodide → [5-(Ethoxycarbonyl)-1H-pyrrol-3-yl]-N,N,N-trimethyl-methanaminium iodide

https://huagongshe.com/reaction/241714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl 4-[(dimethylamino)methyl]-1H-pyrrole-2-carboxylateHCID 66636781—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product[5-(Ethoxycarbonyl)-1H-pyrrol-3-yl]-N,N,N-trimethyl-methanaminium iodideHCID 86662429—

Reaction Steps

To a solution of the product obtained in Step D (0.3 g) in a mixture of tetrahydrofuran (2.2 ml) and CH2Cl2 (2.2 ml) there is added methyl iodide (0.350 ml). A precipitate appears. The reaction mixture is stirred for one hour at ambient temperature and is then left at 4° C. overnight. The reaction mixture is evaporated to dryness and the residue obtained is used directly in the next Step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653073B2
Source datasetuspto-grants-2014_02
ORD IDord-b104b2d59d854f13a34a300aec2077d8
Source noteuspto-grants-2014_02