HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → N-ethoxy-2-bromo-4-butyrolactam
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,4-dibromobutanoyl Bromide | HCID 11289826 | — |
| Reactant | N-ethoxy-2,4-dibromobutyric acid amide | HCID 86632273 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-ethoxy-2-bromo-4-butyrolactam | HCID 67271313 | 37% |
Reaction Steps
137 g of the above-obtained oil containing N-ethoxy-2,4-dibromobutyric acid amide were dissolved in 500 mL of benzene. To the resultant solution, 12 g of sodium hydride were gradually added while cooling the solution to 15° C. to 20° C. After the completion of the addition, ice was added to the resultant reaction solution to decompose excessive sodium hydride. The resultant solution was washed with a saturated saline, followed by drying the solution by magnesium sulfate. The solution was concentrated under a reduced pressure and purified by silica gel-acetone/benzene column chromatography to give 42 g (0.20 mol) of N-ethoxy-2-bromo-4-butyrolactam (with a yield of 37% from 2,4-dibromobutyric acid bromide).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07902383B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-ef6711f74dbd46d0b64c017136d29623 |
| Source note | uspto-grants-2011_03 |