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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593178Generated: October 28, 2026

Sodium Methoxide → 5-(methoxymethyl)-1-methyl-3-nitro-1H-pyrazole

https://huagongshe.com/reaction/593178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
Reactant5-(Bromomethyl)-1-methyl-3-nitro-1H-pyrazoleHCID 58540356—
SolventMethanolHCID 887—
Product5-(methoxymethyl)-1-methyl-3-nitro-1H-pyrazoleHCID 5804420790%

Reaction Steps

A 250-mL single-neck round-bottomed flask equipped with a magnetic stirrer and a reflux condenser was charged with 5-(bromomethyl)-1-methyl-3-nitro-1H-pyrazole (8.8 g, 40 mmol), sodium methoxide (4.3 g, 80 mmol), and methanol (50 mL). The reaction mixture was heated at reflux for 2 h. After this time the reaction was cooled to room temperature and concentrated under reduced pressure. The residue was partitioned between ethyl acetate (60 mL) and water (60 mL). The aqueous layer was separated and extracted with ethyl acetate (2×50 mL). The combined organic layer was washed with brine (50 mL) and dried over sodium sulfate. The drying agent was removed by filtration and the filtrate was concentrated under reduced pressure to afford 336a as a yellow oil (6.1 g, 90%). MS-ESI: [M+H]+ 172.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238655B2
Source datasetuspto-grants-2016_01
ORD IDord-4d3826d2048f4099aa0b3f41df2082a8
Source noteuspto-grants-2016_01