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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486573Generated: October 30, 2026

Methyl iodide → HCID 21803382, compound

https://huagongshe.com/reaction/486573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylamineHCID 7912—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 2758705HCID 2758705—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventHexamethylphosphoramideHCID 12679—
ProductHCID 21803382HCID 2180338270%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 1.6N solution of n-butyllithium in n-hexane was added dropwise within 15 minutes at -70° C. under argon and while stirring to a solution of 7.1 ml of diisopropylamine in 200 ml of absolute tetrahydrofuran. The reaction mixture was stirred at 0° C. for 15 minutes, then again cooled to -70° C., treated with 30 ml of hexamethylphosphoric acid triamide and 9.5 g of 3-(1,3-dioxolan-2-yl)propiophenone, dissolved in 10 ml of absolute tetrahydrofuran and stirred for 15 minutes. After the addition of 3.2 ml of methyl iodide at -70° C. the mixture was brought to room temperature and stirred for 2 hours. The reaction solution was poured on to 100 ml of saturated ammonium chloride solution and extracted once with 200 ml of ethyl acetate and twice with 150 ml of ethyl acetate each time. The organic phases were washed with 100 ml of water, combined, dried with MgSO4 and filtered. The filtrate was concentrated and the residue, 23.4 g of brown oil, was chromatographed on 750 g of silica gel with hexane/ethyl acetate mixtures (4:1 to 2:1). 7.1 g (70%) of 3-(1,3-dioxolan-2-yl)-2-methylpropiophenone were isolated as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292732
Source datasetuspto-grants-1994_03
ORD IDord-98b52b38bcc94eb9801a5890cfe7e21f
Source noteuspto-grants-1994_03