HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384518Generated: October 26, 2026
Acetic Anhydride → 2-Methyl-5-nitrophenyl acetate
https://huagongshe.com/reaction/1384518
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Methyl-5-nitrophenol | HCID 93576 | — |
| Product | 2-Methyl-5-nitrophenyl acetate | HCID 17934259 | 100% |
Reaction Steps
To a mixture of 2-methyl-5-nitrophenol (2.5 g, 16.3 mmol) and 1M aqueous sodium hydroxide (24.5 ml) was added at ambient temperature acetic anhydride (1.9 ml, 20.3 mmol). The mixture was stirred for 40 minutes, the solid was filtered off and the filtrate extracted with ethyl acetate. The organic layers were combined, washed with an aqueous saturated sodium chloride solution, dried (MgSO4) and evaporated to yield 2-acetoxy-4-nitrotoluene (3.1 g, 100%). A mixture of this material (3.1 g, 15.9 mmol) and 10% palladium-on-charcoal catalyst (0.12 g) in ethyl acetate (50 ml) was stirred at ambient temperature under an atmosphere of hydrogen for 2 hours. The catalyst was filtered off and the filtrate evaporated to give 3-acetoxy-4-methylaniline (2.45 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06258951B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-cf3a8981d60c4ce490901721bcf1a8c6 |
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| Source note | uspto-grants-2001_07 |
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