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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373616Generated: October 30, 2026

Methyl iodide → Methyl 2-(3-nitrophenyl)propanoate

https://huagongshe.com/reaction/2373616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 2-(3-nitrophenyl)acetateHCID 526967—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(3-nitrophenyl)propanoateHCID 1305427233.9%

Reaction Steps

A solution of lithium hexamethyldisilazide (1M, hexane, 1.0 eq., 21.5 ml) was added dropwise to a stirred solution of methyl (3-nitrophenyl)acetate (4.2 g) in THF (30 ml) at −30□ C. The mixture was warmed to 0□ C. and re-cooled to −30□ C. then iodomethane (1.0 equiv., 3.0 g.) was added. The solution was warmed to room temperature and poured into aqueous ammonium chloride solution and extracted with ethyl acetate. The combined organic phases were washed with brine, dried over sodium sulfate and concentrated. The crude was purified using chromatography (SiO2, SPE) using cyclohexane/ethyl acetate (80/20) as eluent to afford the title compound as yellow liquid (1.50 g, 30% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459456B2
Source datasetuspto-grants-2008_12
ORD IDord-daf598aa33064b5d9b99f21a44611723
Source noteuspto-grants-2008_12