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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989592Generated: October 29, 2026

Methanol → N-(5-Nitro-2-methoxyphenyl)-2,2,5-trimethyl-beta-oxo-1,3-dioxane-5-propanamide

https://huagongshe.com/reaction/989592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-Methoxy-5-nitroanilineHCID 7447—
ReactantM-XyleneHCID 7929—
ReactantHCID 53655320HCID 53655320—
SolventOctaneHCID 356—
ProductN-(5-Nitro-2-methoxyphenyl)-2,2,5-trimethyl-beta-oxo-1,3-dioxane-5-propanamideHCID 19895265—

Reaction Steps

2Methoxy-5-nitroaniline (63.06 g, 0.375 mol) and methyl 2,2,5-trimethyl-b-oxo-1,3-dioxane-5-propanoate (90.0 g, 0.391 mol) were dispersed in n-octane (500 mL) and m-xylene (100 mL) in a 2-liter three-necked flask. The mixture was heated at the boiling point while methanol was continuously removed by a very slow nitrogen sweep. After 2 hr of heating the solution was allowed to cool slowly with good stirring; the yellow-orange precipitate which formed was filtered and allowed to air dry. The crude precipitate was dissolved in ethyl ether and extracted with dilute hydrochloric acid, after which the ethereal solution was washed once with dilute sodium bicarbonate, once with water, the organic and aqueous layers separated, and the organic layer dried over magnesium sulfate. The mixture was filtered and the excess solvent removed in vacuo. The residue was recrystallized from ethyl alcohol, m.p. 113-5° C.; H-NMR was consistent. Elemental analysis calculated for C17H22N5O7: C, 55.73; H, 6.05; N, 7.65. Found: C, 55.64; H. 6.14; N, 7.53.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458521B1
Source datasetuspto-grants-2002_10
ORD IDord-e37d5261a0a24af69b8ff5a4c9b992ae
Source noteuspto-grants-2002_10