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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65204Generated: October 29, 2026

Benzene → 2-Nitroxymethylpyridine nitrate

https://huagongshe.com/reaction/65204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantNitric AcidHCID 944—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 70400506HCID 70400506—
SolventHexaneHCID 8058—
Product2-Nitroxymethylpyridine nitrateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04613608
Source datasetuspto-grants-1986_09
ORD IDord-a96a1a5f8e014a1883c990e494b0239f
Source noteuspto-grants-1986_09