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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35180Generated: October 30, 2026

Acetone → HCID 15599400, compound

https://huagongshe.com/reaction/35180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantFormaldehydeHCID 712—
ReactantAcetic AnhydrideHCID 7918—
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantHCID 15035895HCID 15035895—
ProductHCID 15599400HCID 1559940081%

Reaction Steps

3,4-Dihydro-7-methyl-6-(1-oxopropyl)-3-oxo-1,4(2H)-benzoxazine (23.7 g) was added to a mixture of 13 g of dimethylamine hydrochloride and 15 ml of 37% aqueous formaldehyde solution in 68 ml of acetic anhydride. After heating on a steam bath for three hours, 50 ml of acetone was added and heating was continued for 15 minutes. The solvents were removed by evaporation at reduced pressure and the residue was dissolved in 1N HCl and washed with ethyl acetate. The aqueous layer was basified with sodium hydroxide and the resultant crystals were collected by filtration. This product was dissolved in 500 ml of acetone and 10 ml of iodomethane were added. After heating at reflux overnight, the solid which formed was collected by filtration and washed with acetone. The product was dissolved in 400 ml of 50% aqueous methanol and 18 g of potassium cyanide in 200 ml of water was added. After stirring overnight at room temperature, the solid was collected and washed with water. The damp filter cake was suspended in 500 ml of 6N HCl and heated at reflux for 1.5 hours. Upon cooling a white precipitate formed which was collected by filtration and washed with water to give 19.4 g (81% yield) of the title compound, mp 169.5°-172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766118
Source datasetuspto-grants-1988_08
ORD IDord-d2e6d3197efe44ee82a1ae6ef883fc30
Source noteuspto-grants-1988_08