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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754408Generated: November 2, 2026

Methyl iodide → HCID 86704466, compound

https://huagongshe.com/reaction/1754408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 13115685HCID 13115685—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86704466HCID 8670446655.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Hexahydro-5,5-dimethylindolizin-7(1H)-one (racemic) (1.41 g, 8.43 mmol) was dissolved in dry THF (50 ml); the flask was flushed with nitrogen and cooled to −78° C. LDA (5.9 ml, 11.8 mmol) was added via syringe and stirred for 30 minutes. Subsequently, neat methyl iodide (1.30 ml, 21.1 mmol) was added via syringe. The clear, pale yellow solution was stirred overnight and allowed to warm to room temperature. The reaction was then quenched with a saturated NH4Cl solution and extracted with ethyl acetate (3×40 ml). The organic phases were passed through a plug of MgSO4 and solvents were evaporated in vacuo. The crude product (849 mg) was obtained in form of a yellow-brown oil and used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169249B2
Source datasetuspto-grants-2015_10
ORD IDord-537deec68c334cfbacdf8fcd0d86037e
Source noteuspto-grants-2015_10