HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393626Generated: October 25, 2026
Acetic Anhydride → 2-Methyl-5-nitrophenyl acetate
https://huagongshe.com/reaction/393626
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) at ambient temperature was added acetic anhydride (1.9 ml 120.3 mmol). The mixture was stirred for 40 minutes, the solid was removed by filtration and the filtrate was extracted with ethyl acetate. The organic layers were combined, washed with an aqueous saturated sodium chloride solution, dried (MgSO4) and the volatiles were removed by evaporation 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 hydrogen for 2 hours. The catalyst was removed by filtration and the volatiles were removed by evaporation 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 | US06809097B1 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-f7ac411c3c0e4f53bb0836d225740d08 |
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| Source note | uspto-grants-2004_10 |
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