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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370139Generated: October 29, 2026

Isocyanatocarbonyl chloride → 8-phenyl-7,8-dihydropyrano[3,4-e][1,3]oxazine-2,4(3H,5H)-dione

https://huagongshe.com/reaction/2370139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsocyanatocarbonyl chlorideHCID 119708—
Reactant3-Phenyloxan-4-oneHCID 58075264—
SolventEthyl AcetateHCID 8857—
Product8-phenyl-7,8-dihydropyrano[3,4-e][1,3]oxazine-2,4(3H,5H)-dioneHCID 5807530661.8%

Reaction Conditions

Temperature58 °C

Reaction Steps

A mixture of 3-phenyldihydro-2H-pyran-4(3H)-one (Intermediate I(2)) (3 g, 17.02 mmol) and carbonisocyanatidic chloride (10.48 g, 29.8 mmol) in a sealed tube was heated to 58° C. and stirred for 1 h. The mixture was then brought to 130° C. and stirred for an additional 2 h. The reaction turned black during this time. After cooling to RT, the tar was taken up in EtOAc (100 mL). The resulting solution was washed with saturated aqueous sodium bicarbonate (2×50 mL), brine (50 mL), dried over MgSO4, filtered and concentrated in vacuo. Purification by flash chromatography (Silica, EtOAc/Hexanes) gave 8-phenyl-7,8-dihydropyrano[3,4-e][1,3]oxazine-2,4(3H,5H)-dione (2.58 g, 10.52 mmol, 61.8% yield) as a brown solid. LC-MS (M+H)+=246.0. 1H NMR (500 MHz, MeOD) δ ppm 7.34-7.41 (4 H, m), 7.29-7.34 (1 H, m), 4.42-4.63 (2 H, m), 4.08-4.15 (1 H, m), 3.94 (1 H, dd, J=11.44, 4.12 Hz), 3.85 (1 H, ddd, J=4.20, 2.44, 2.21 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710061B2
Source datasetuspto-grants-2014_04
ORD IDord-bdce809963dd48f1915d179277b75f46
Source noteuspto-grants-2014_04