Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Acetone Cyanohydrin | HCID 6406 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-Methoxy-2,2,6,6-tetramethylpiperidin-4-one | HCID 10976193 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 67127982 | HCID 67127982 | — |
Reaction Steps
0.61 g of 1-Methoxy-2,2,6,6-tetramethyl-piperidin-4-one and 299 mg acetone cyanhydrine are dissolved in 1.76 g acetic acid and 0.7 g conc. sulfuric acid is added. The reaction mixture is stirred at 70° C. for 18 h. The reaction mixture is added to 40 ml saturated NaHCO3 solution, and extracted with 40 ml ethyl acetate. The organic phase is washed with H2O and subsequently dried over sodium sulfate. The solvent is removed in vacuo to leave 0.61 g of a tan residue. The residue is recrystallized from hexane to yield 0.29 g product. White solid, mp. 130° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045480B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-7ac05810c621473cabfd03977f4345da |
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| Source note | uspto-grants-2015_06 |
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