Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734564Generated: October 27, 2026

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

https://huagongshe.com/reaction/734564

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 numberUS07592346B2
Source datasetuspto-grants-2009_09
ORD IDord-3008fcfa18f64dfe89163dcda15b5ee4
Source noteuspto-grants-2009_09