HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 19420321, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,4-Dibromo-2-butanol | HCID 29570 | — |
| Reactant | 4-Acetoxy-2-azetidinone | HCID 119981 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 19420321 | HCID 19420321 | — |
Reaction Steps
A mixture of 1,4-dibromo-2-butanol (5.8 ml), 4-Acetoxyazetidinone (6.46 g), Palladium acetate (450 mg), Triethylamine (7 ml) and dry Benzene (75 ml) was stirred at room temperature under nitrogen for 23 hrs. Resulting solid was filtered off and filtrate was washed with water, brine and then dried over Magnesium sulfate. The residual oil, after evaporation, was purified by column chromatography using Hexane and Ethyl acetate (2:1) and the title compound was obtained. Yield: 5.88 g (78%). NMR (CDCl3): 2.05-2.17 (2H, m), 2.87-3.27 (2H, m), 3.42-3.60 (4H, m), 3.90-4.02 (1H, m), 5.23-5.33 (1H, m), 6.53 (1H, br, s). IR (Neat), cm-1 : 3260, 1771.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05561126 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-ff00a70806a14de29c5e656dc5205010 |
| Source note | uspto-grants-1996_10 |