HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → HCID 10568063, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-benzyl-3-hydroxy-2,3-dihydro-1H-isoindol-1-one | HCID 3240743 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10568063 | HCID 10568063 | 73.2% |
Reaction Steps
To a solution of compound 20 (2.0 g, 8.4 mmol) in DMF (28 mL) at room temperature was added sodium hydride (235 mg, 8.8 mmol) and ethyl bromoacetate (1.03 mL, 9.2 mmol) and the resulting reaction mixture was allowed to stir at room temperature for 18 hours. The reaction mixture is poured onto water and extracted with ethyl acetate (3×100 mL). The combined ethyl acetate extracts were dried over anhydrous sodium sulfate and concentrated in vacuo to provide 2 g of 21 as a clear oil (2.73 g theoretical, 73% yield)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531671B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-38fb03222e0e4663bb5f35533d62ecd8 |
| Source note | uspto-grants-2009_05 |