HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65204Generated: October 29, 2026
Benzene → 2-Nitroxymethylpyridine nitrate
https://huagongshe.com/reaction/65204
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 70400506 | HCID 70400506 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-Nitroxymethylpyridine nitrate | HCID 86740295 | — |
Reaction Steps
Fuming nitric acid (4.1 ml) was added dropwise to acetic anhydride (13.5 ml) with stirring at 5° to 10° C. After the mixture was stirred for 30 minutes at 5° C., 2-hydroxymethylpyridine nitrate (3.3 g) was added in some portions thereto. The resulting mixture was stirred for 3 hours at 0° to 5° C. A mixture of benzene (15 ml) and n-hexane (30 ml) was added thereto. The mixture formed two layers. The upper layer was separated and discarded while the remaining lower layer was again treated with a mixture of benzene (10 ml) and n-hexane (10 ml). After the separation of the layers, the lower layer was again separated, mixed with benzene (10 ml) and made homogeneous with isopropyl alcohol (10 ml). The resulting mixture was allowed to stand overnight in a refrigerator to give crystals. The crystals were collected by filtration and washed with diethyl ether to give white crystals of 2-nitroxymethylpyridine nitrate (2.4 g), mp. 75° to 77° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04613608 |
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| Source dataset | uspto-grants-1986_09 |
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| ORD ID | ord-a96a1a5f8e014a1883c990e494b0239f |
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| Source note | uspto-grants-1986_09 |
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