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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180561Generated: November 3, 2026

Methyl iodide → HCID 22491048, compound

https://huagongshe.com/reaction/2180561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 22491033HCID 22491033—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22491048HCID 22491048—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 1-(3-ethoxy-5,5-dimethyl-5,6-dihydro-naphthalen-2-yl)-ethanone (Compound A-25, 0.17 g, 0.68 mmol) in THF (33 mL) at −78° C. was added lithium diisopropylamide (1.5 M in cyclohexane, 0.55 mL 0.82 mmol). The cold bath was removed and the mixture was stirred for 2 h. The mixture was cooled to −78° C. again and methyl iodide (0.13 mL, 2.04 mmol) was added. The mixture was stirred at room temperature for 12 h then quenched with a saturated solution of NH4Cl and extracted with diethyl ether. The combined ethereal layers were washed with water, brine, dried (Na2SO4), filtered and concentrated in vacuo. The crude residue was purified by flash chromatography (silica gel, 2% ethyl acetate in hexane) to give the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06887896B1
Source datasetuspto-grants-2005_05
ORD IDord-8d580488ada340a4b5bb9f4957c7ac4e
Source noteuspto-grants-2005_05