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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 914944Generated: October 30, 2026

2-Nitropropane → HCID 22038580, compound

https://huagongshe.com/reaction/914944

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitropropaneHCID 398—
ReactantMethyl iodideHCID 6328—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 22038579HCID 22038579—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 22038580HCID 2203858092%

Reaction Steps

A 0° C. solution of 3-dimethylaminomethyl-1H-7-azaindole hydroiodide (10 g, 33 mmol) in 46 ml of methanol and 46 ml of 2-nitropropane is treated with methyl iodide (2.15 ml, 35 mmol) and solid sodium methoxide (3.65 g, 68 mmol) sequentially. The resulting mixture is allowed to warm to ambient temperature, and, after stirring overnight, the reaction mixture is diluted with ethyl acetate (100 ml) and saturated aqueous NH4Cl solution (100 ml). The aqueous layer is extracted with ethyl acetate (2×100 ml), and the combined organic layers are dried over Na2SO4 and concentrated in vacuo to give 3-(2-methyl-2-nitropropyl)-1H-7-azaindole in 92% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265127B2
Source datasetuspto-grants-2007_09
ORD IDord-bf1e53cbdc9f4390a7030884cf8ba856
Source noteuspto-grants-2007_09