HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoacetic Acid → (2-Benzyl-3-oxo-2,3-dihydro-1H-isoindol-1-yloxy)-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoacetic Acid | HCID 6227 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-benzyl-3-hydroxy-2,3-dihydro-1H-isoindol-1-one | HCID 3240743 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Benzyl-3-oxo-2,3-dihydro-1H-isoindol-1-yloxy)-acetic acid | HCID 10613926 | 40.2% |
Reaction Steps
To a suspension of sodium hydride (1.1 g, 38.5 mmol) in THF (30 mL) at room temperature was added a solution of compound 20 (2.0 g, 8.37 mmol) in THF (15 mL) and the resulting reaction mixture was allowed to stir at room temperature for 1 hour. Thereafter a solution of bromo acetic acid (2.68 g, 19.25 mmol) in THF (5 mL) was added dropwise 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 ether (3×100 mL) and the combined ethyl ether extracts were dried over anhydrous sodium sulfate and concentrated in vacuo. Chromatography (SiO2, 20 to 70% EtOAc-Hexanes eluant) provided 1.0 g of 22 as a clear oil (2.48 g, theoretical, 40% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531671B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-5eea9b605c91468b82e43765d99e2958 |
| Source note | uspto-grants-2009_05 |