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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440766Generated: November 2, 2026

Ethyl Acetate → HCID 54169012, compound

https://huagongshe.com/reaction/1440766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium HydroxideHCID 14797—
Reactant1-IodopropaneHCID 33643—
ReactantHCID 21475768HCID 21475768—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 54169012HCID 5416901222.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

1.3 g (11.4 mmol) of 2-amino-6H-1,3-thiazine was dissolved in 4 ml of dimethylformamide, and 2.4 g (14.1 mmol) of n-propyl iodide was added thereto. The mixture was heated at 50° C. for one hour and then stirred at room temperature overnight. To the reaction solution, 100 ml of ethyl acetate was added, and the mixture was stirred and then left to stand still. Then, the ethyl acetate layer was separated and removed by decantation. Then, the residual oily substance was dissolved in 50 ml of methanol, and 30 ml of a methanol solution containing 0.75 g (11.4 mmol) of 85% potassium hydroxide, was added thereto at room temperature. The mixture was further stirred at the same temperature for one hour, and then methanol was distilled off under reduced pressure. To the residue, 60 ml of chloroform was added, and insoluble matters were removed by filtration. Then, the filtrate was concentrated under reduced pressure. The residual oily substance was purified by alumina column chromatography (eluent: chloroform) to obtain 0.4 g of 3,6-dihydro-3-n-propyl-2H-1,3-thiazin-2-imine as an oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05500406
Source datasetuspto-grants-1996_03
ORD IDord-60975d7e4aa04713aa149342d66a2567
Source noteuspto-grants-1996_03