Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | HCID 21394477 | HCID 21394477 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 21394499 | HCID 21394499 | — |
Reaction Steps
19.1 g (0.1 mole) of 2,2,6,6-tetramethyl-1-aza-4-thiacyclohexane-4,4-dioxide is added, with ice cooling, to 20 ml of 5N hydrochloric acid; 6.5 g of potassium cyanide is added and then in ca. 20 minutes, with good stirring, an addition made dropwise of 12.5 g of a 30% formaldehyde solution. The reaction mixture is subsequently stirred for 15 hours at 45° C. After cooling, the precipitate is filtered off under suction, washed with water, dried, and recrystallised from toluene/hexane to obtain 1-cyanomethyl-2,2,6,6-tetramethyl-1-aza-4-thiacyclohexane-4,4-dioxide (11), M.P. 188° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04061631 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-ec25f525ffca4c5fa6cab510ea0dd86e |
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| Source note | uspto-grants-1977_12 |
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