Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | M-Cresol | HCID 342 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 2-Nitrobenzaldehyde | HCID 11101 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Nitrobenzaldehyde | HCID 7449 | — |
Reaction Steps
190.0 g of water-moist m-nitrobenzaldehyde (containing 163.0 g of crude nitrobenzaldehyde of the composition: 1.5% by weight of o-isomer; 2.3% by weight of p-isomer; 96.2% by weight of m-isomer) were suspended in 445 g of water and 20.0 g of an emulsifier, which was prepared by condensation of m-cresol, formaldehyde, sodium sulphite and 2-naphthol-6-sulphonic acid, were added. The suspension was heated to 60° C. and adjusted to pH 10.4 using NaOH. The mixture was subsequently heated to reflux and stirred under reflux for 30 minutes. It was then cooled to 40° C., stirred at 40° C. for 2.5 hours and filtered off with suction. The filtered material was washed with water and freshly filtered with suction. After drying, 141.7 g of m-nitrobenzaldehyde were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04910345 |
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| Source dataset | uspto-grants-1990_03 |
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| ORD ID | ord-cb3142b7d3304a07a910c2a73432db3d |
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| Source note | uspto-grants-1990_03 |
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