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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252729Generated: November 3, 2026

Cyclohexane → HCID 13827094, compound

https://huagongshe.com/reaction/1252729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexaneHCID 8078—
ReactantHCID 13827089HCID 13827089—
CatalystPalladiumHCID 23938—
SolventBenzeneHCID 241—
ProductHCID 13827094HCID 1382709447%

Reaction Steps

7-Nitro-2-ethoxy-4H-3,1-benzoxazin-4-one (1 gm, 4.2 m mol.), 10% Pd-C (1 gm), and cyclohexane (2.5 ml) were refluxed in dry benzene (50 ml) under anhydrous conditions for 3 hours. The hot reaction mixture was filtered immediately through celite and the catalyst on celite was washed with hot benzene (25 ml). The combined filtrate was evaporated to dryness under reduced pressure. The residue was stirred in anhydrous ether (30 ml) to give 410 mg (47%) of the title compound, 7-amino-2-ethoxy-4H-3,1-benzoxazin-4-one, as a pale yellow powder, after filtration. The product can be further purified by chromatography on silica gel column, if necessary (silica gel 60; EtOAc:pet. ether=1:2); m. p. 185°-187° C.; IR (KBr): νmax 3425, 3330 cm-1 (NH2), 1740 cm-1 (C=O), 1640 cm-1 (C=N); H'NMR (CDCl3): δ1.43 ppm (t, J=7.1 Hz, 3H, OCH2CH3), 4.30 ppm (b, 2H, NH2), 4.75 ppm (q, J=7.1 Hz, 2H, OCH2CH3), 6.5-7.98 ppm (m, 3H, aromatic protons).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04745116
Source datasetuspto-grants-1988_05
ORD IDord-b75ce80845174af8b6c18f89ac4773ac
Source noteuspto-grants-1988_05