Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Acetoxy-3-methoxybenzaldehyde | HCID 251703 | — |
| Product | HCID 21783433 | HCID 21783433 | — |
Reaction Steps
42 (42.0 g, 0.22 mol) was added portionwise as a finely ground powder over 1 h to a solution of concentrated sulphuric acid (28 mL) in 100% nitric acid (140 mL) at −20° C. During the addition, the reaction temperature was maintained at around −15° C. The reaction mixture was stirred at −5° C. for a further 40 min, then poured into to ice/water (1 L) and extracted rapidly with toluene (2×). The organic phase was washed successively with 0.25 M NaHCO3 aq. water and brine, dried (Na2SO4) and evaporated to dryness to give crude product (19.8 g) as a yellow oil, which was shown by NMR to contain ˜60% nitro-compounds. Purification of 8 g of this material by column chromatography (three times, SiO2, first eluting with 1:9 EtOAc:cyclohexane, then with 3:7 EtOAc:cyclohexane and finally with 1:1 EtOAc:cyclohexane) gave 43 (2.53 g) in (˜80% purity) together with 2-hydroxy-3-methoxy-4-nitrobenzaldehyde (˜10%). The product was used as such in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198302B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-dfe6e49bf0174b03ac455a26bf1deeda |
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| Source note | uspto-grants-2012_06 |
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