HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Piperidinone, 3,5-dibromo-2,2,6,6-tetramethyl-, hydrobromide (1:1) → 2,2,5,5-Tetramethyl-3-pyrroline-3-carboxylic Acid (5-Hydroxy-2,2-dimethyl-1,3-dioxepan-6-yl)-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Piperidinone, 3,5-dibromo-2,2,6,6-tetramethyl-, hydrobromide (1:1) | HCID 89251 | — |
| Reactant | 6-Amino-2,2-dimethyl-1,3-dioxepan-5-ol | HCID 3387444 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2,2,5,5-Tetramethyl-3-pyrroline-3-carboxylic Acid (5-Hydroxy-2,2-dimethyl-1,3-dioxepan-6-yl)-amide | HCID 54204802 | — |
Reaction Steps
Analogously to Example 7, 78.79 g (200 mmol) of 3,5-dibromo-2,2,6,6-tetramethylpiperidin-4-one hydrobromide, 69.34 g of potassium tert-butylate, and 35.47 g (220 mmol) of 6-amino-2,2-dimethyl-1,3-dioxepan-5-ol are reacted in 800 ml of isopropanol and then extracted with dichloromethane. Yield: 37.66 g (60.3% of theory) of 2,2,5,5-tetramethyl-3-pyrroline-3-carboxylic acid (5-hydroxy-2,2-dimethyl-1,3-dioxepan-6-yl)amide which, crystallized from diethyl ether/hexane, shows a melting point of 125°-127° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04845090 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-c2577182005a46319ea49a89d9fd366e |
| Source note | uspto-grants-1989_07 |