HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424286Generated: October 25, 2026
Nitromethane → 4-Methoxy-beta-nitrostyrene
https://huagongshe.com/reaction/424286
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitromethane | HCID 6375 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Reactant | Hydrate;hydrochloride | HCID 21885828 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Methoxy-beta-nitrostyrene | HCID 229843 | — |
Reaction Steps
p-Methoxybenzaldehyde (11.19 g, 82.2 mmol) and nitromethane (5.0 g, 82.2 mmol) were dissolved in methanol (20 mL) in a two-necked flask equipped with a thermometer and a pressure-equalizing dropping funnel. NaOH (4.27 g, 0.107 mol) in ice/water (10 mL) was added dropwise to the solution keeping the temperature below 15° C. A fine slurry formed during addition and additional methanol was added to allow efficient stirring. After the addition the reaction mixture was diluted with ice/water and the resulting clear solution was added dropwise to a solution of HCl/H2O (40 mL/60 mL); a yellow precipitate formed during the addition. The precipitate was filtered on a buchner funnel and crystallized from methanol obtaining 4-methoxy-β-nitrostirene (10.66 g, 72%). Yellow needles. M.p. 57-58° C. ESI-MS: 180 (MH±); (Calc. for C9H9NO3: 179 u.m.a.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08105567B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-87d1d61c7459494ea25f92ab01132837 |
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| Source note | uspto-grants-2012_01 |
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