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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504907Generated: November 1, 2026

Methyl iodide → HCID 117974160, compound

https://huagongshe.com/reaction/1504907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 12218077HCID 12218077—
ProductHCID 117974160HCID 11797416094%

Reaction Steps

N-(2-methylcyclohexyl)pyrrolidine as synthesized in Example 3 above, was quaternized with methyl iodide using the procedure described in example 4 with the exception of using N-(2-methylcyclohexyl)pyrrolidine in place of N-cyclohexylpyrrolidine. The quaternization procedure afforded the desired N-methyl-N-(2-methylcyclohexyl)pyrrolidinium iodide in 94% yield as an off-white solid. This N-methyl-N-(2-methylcyclohexyl)pyrrolidinium iodide was ion-exchanged with BIO-RAD AGR 1-X* resin as described in example 4 above. The ion-exchange procedure afforded the hydroxide solution of N-methyl-N-(2-methylcyclohexyl)pyrrolidinium cation in 91% yield as determined by titration analysis on a small aliquot.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216911B2
Source datasetuspto-grants-2015_12
ORD IDord-e98af97f3a084984a5cea7881a296738
Source noteuspto-grants-2015_12