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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463808Generated: October 31, 2026

Methyl sulfate(1-) → 3,5-Dimethyl-1,3,5-oxadiazinane-2,4,6-trione

https://huagongshe.com/reaction/463808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl sulfate(1-)HCID 4694097—
Reactant3-Methyl-1,3,5-oxadiazinane-2,4,6-trioneHCID 20265335—
SolventWaterHCID 962—
SolventCarbon TetrachlorideHCID 5943—
Product3,5-Dimethyl-1,3,5-oxadiazinane-2,4,6-trioneHCID 1245532392%

Reaction Steps

The process disclosed in example 1 is used, except that the solvent is not distilled. 15.1 g of methyl sulfate (0.12 mole) are added to the solution of 3-methyl-1,3,5-oxadiazine-2,4,6-trione. The solvent is evaporated after 10 minutes of reaction at a temperature of 25° C. After washing with water and carbon tetrachloride, 14.6 g of 3,5-dimethyl-1,3,5-oxadiazine-2,4,6-trione (yield: 92%) which is a symmetrical disubstituted 1,3,5-oxadiazine trione are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04544743
Source datasetuspto-grants-1985_10
ORD IDord-b4e8bd624fac475eb35b2251357ce230
Source noteuspto-grants-1985_10