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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514648Generated: October 30, 2026

Methyl iodide → HCID 117951634, compound

https://huagongshe.com/reaction/514648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHCID 13184333HCID 13184333—
ProductHCID 117951634HCID 11795163494%

Reaction Steps

Referring to Scheme 4 below, N-(3-methylcyclohexyl)pyrrolidine prepared in Example 2 above was quaternized with methyl iodide in a similar fashion to the procedure described in in example 3. The quaternization afforded the desired N-methyl-N-(3-methylcyclohexyl)pyrrolidinium iodide in 94% yield. The resulting iodide salt was exchanged with Bio-Rad AG 1-X8 ion-exchange resin as described in example 3 to give N-methyl-N-(3-methylcyclohexyl)pyrrolidinium hydroxide in 98% yield (titration analysis).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108856B2
Source datasetuspto-grants-2015_08
ORD IDord-3ca60812278b4934a7badcf69bf7d551
Source noteuspto-grants-2015_08