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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481490Generated: October 25, 2026

Methyl iodide → 4-(1-(N-acetyl-N-methylamino)cyclopropyl)anisole

https://huagongshe.com/reaction/481490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant4-(1-(N-Acetylamino)cyclopropyl)anisoleHCID 19066431—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventAmmonium ChlorideHCID 25517—
Product4-(1-(N-acetyl-N-methylamino)cyclopropyl)anisoleHCID 1906649773.4%

Reaction Steps

To a stirred suspension of 60% sodium hydride (234 mg, 5.85 mmol) (washed with pentane) in dry DMF (20 ml) was added Compound 8 (1.00 g, 4.87 mmol) portionwise at room temperature. After 15 min., to this was added iodomethane (1.04 g, 7.31 mmol) at same temperature. The reaction mixture was stirred at room temperature for 2 h. The mixture was diluted with sat. NH4Cl aq. (20 ml)-H2O (20 ml) and extracted with toluene-AcOEt (1:2). The combined solution was washed with water and brine, dried(MgSO4) and concentrated in vacuo to give crude product (1.05 g) as a yellow solid. The crude product was recrystallized from hexane-ethyl acetate to give Compound 9 (784 mg, 73%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789423
Source datasetuspto-grants-1998_08
ORD IDord-93e42b44c33b4d50a7f666f8061788fc
Source noteuspto-grants-1998_08