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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 5-(Bromomethyl)-1-methyl-3-nitro-1H-pyrazole | HCID 58540356 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-(methoxymethyl)-1-methyl-3-nitro-1H-pyrazole | HCID 58044207 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238655B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-4d3826d2048f4099aa0b3f41df2082a8 |
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| Source note | uspto-grants-2016_01 |
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