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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1577754Generated: November 1, 2026

Methyl Isocyanate → N-(5,5,7,7-Tetramethyl-4,5,6,7-tetrahydrobenzothiazol-2-YL)-N'-methylurea

https://huagongshe.com/reaction/1577754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl IsocyanateHCID 12228—
ReactantIsocyanateHCID 105034—
Reactant4,5,6,7-tetrahydro-5,5,7,7-tetramethyl-2-BenzothiazolamineHCID 12783348—
SolventEthyl AcetateHCID 8857—
ProductN-(5,5,7,7-Tetramethyl-4,5,6,7-tetrahydrobenzothiazol-2-YL)-N'-methylureaHCID 12783349—

Reaction Steps

2-Amino-5,5,7,7-tetramethyl-4,5,6,7-tetrahydrobenzothiazole (21 grams; 0.1 mole) was dissolved in ethyl acetate (100 ml) and the solution charged into a glass reaction vessel fitted with a mechanical stirrer and themometer. Methyl isocyanate (6.2 grams 0.11 mole) was added dropwise to this solution over a period of 30 minutes. The temperature of the reactants was at about 20°-25° C. during the addition. At the conclusion of the isocyanate addition, stirring was continued at room temperature for a period of about 2 hours. The desired product, 2-amino-5,5,7,7-tetramethyl-4,5,6,7-tetrahydrobenzothiazole, a solid, was then filtered from the reaction mixture and air dried. Its melting point was greater than 250° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04289524
Source datasetuspto-grants-1981_09
ORD IDord-19c871d1ec5f49a3b2e5bf323111be6b
Source noteuspto-grants-1981_09