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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844735Generated: October 31, 2026

Methyl iodide → Cyclohexyl(1-methyl-1H-pyrrol-2-yl)methanone

https://huagongshe.com/reaction/1844735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantCyclohexyl(1H-pyrrol-2-yl)methanoneHCID 13432026—
SolventDimethylformamideHCID 6228—
ProductCyclohexyl(1-methyl-1H-pyrrol-2-yl)methanoneHCID 1404340580%

Reaction Steps

Compound 25a (2.0 g, 11.3 mmol dissolved dry DMF) was added portionwise to the mixture of NaH (60%; 0.904 g, 22.6 mmol) and dry DMF (200 mL) and the mixture was stirred for 30 min at rt, then MeI (1.9 g, 11.6 mmol) was added at 0° C. The stirred mixture was allowed to stand at rt for 2 h, poured slowly into ice-water and extracted with EA. The organic phase was dried (MgSO4), evaporated and purified by CC to give compound 25b (1.73 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946446B2
Source datasetuspto-grants-2015_02
ORD IDord-9d8b94d06ea343abb998c87073ac973e
Source noteuspto-grants-2015_02