HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1577755Generated: November 4, 2026
Sulfuric Acid → 3-(5,5,7,7-Tetramethyl-4,5,6,7-tetrahydro-benzothiazol-2-yl)-5methyltetrahydro-1,3,5-oxadiazin-4-one
https://huagongshe.com/reaction/1577755
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1,3,5-Trioxane | HCID 8081 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-(5,5,7,7-Tetramethyl-4,5,6,7-tetrahydrobenzothiazol-2-YL)-N'-methylurea | HCID 12783349 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(5,5,7,7-Tetramethyl-4,5,6,7-tetrahydro-benzothiazol-2-yl)-5methyltetrahydro-1,3,5-oxadiazin-4-one | HCID 12783350 | — |
Reaction Steps
Sulfuric acid, 85% concentration (40 grams) was charged into a glass reaction vessel fitted with a mechanical stirrer and a thermometer and was cooled to about 5° C. N-(5,5,7,7-tetramethyl-4,5,6,7-tetrahydrobenzothiazol-2-yl)-N'-methylurea (4.1 grams; 0.015 mole) and s-trioxane (1.4 grams, 0.015 mole) were added portionwise, with stirring, to the cold sulfuric acid. Stirring was continued for a period of about 16 hours at a temperature of about 20°-25° C. The reaction mixture was then diluted 1:1 with water and neutralized with aqueous 40% sodium hydroxide. The neutralized mixture was filtered and the solid obtained was washed with 3-100 ml portions of water and air dried to yield the desired product 3-(5,5,7,7-tetramethyl-4,5,6,7-tetrahydro-benzothiazol-2-yl)-5methyltetrahydro-1,3,5-oxadiazin-4-one as a solid having a melting point of 138°-140° C. Elemental analysis: Theory: C: 58.22%; H: 7.49%; N: 13.58%; Found: C:57.53%; H: 7.57%; N: 13.61 %.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04289524 |
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| Source dataset | uspto-grants-1981_09 |
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| ORD ID | ord-239bc35c0fd74dc28e469024ecd42dbb |
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| Source note | uspto-grants-1981_09 |
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