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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504906Generated: November 1, 2026

Iodoethane → HCID 117951629, compound

https://huagongshe.com/reaction/1504906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantHCID 13184333HCID 13184333—
ProductHCID 117951629HCID 11795162985%

Reaction Steps

N-(3-methylcyclohexyl)pyrrolidine prepared in example 2 above was quaternized with ethyl iodide in a similar fashion to the procedure described in example 6 with the exception of using ethyl iodide in place of methyl iodide. The quaternization afforded the desired N-ethyl-N-(3-methylcyclohexyl)pyrrolidinium iodide in 85% yield. The resulting N-ethyl-N-(3-methylcyclohexyl)pyrrolidinium iodide salt was exchanged with Bio-Rad AG 1-X8 ion-exchange resin as described in example 4 to give N-methyl-N-(3-methylcyclohexyl)pyrrolidinium hydroxide in 88% yield (by titration).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216911B2
Source datasetuspto-grants-2015_12
ORD IDord-f0452a59eec14834b129719318464280
Source noteuspto-grants-2015_12