HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → Dibenzyl (S)-2,5-dihydro-1H-pyrrole-1,2-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | (S)-2,5-Dihydro-pyrrole-1,2-dicarboxylic acid 1-benzyl ester | HCID 10422063 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Dibenzyl (S)-2,5-dihydro-1H-pyrrole-1,2-dicarboxylate | HCID 11142303 | — |
Reaction Steps
To a solution of (S)-2,5-dihydro-pyrrole-1,2-dicarboxylic acid 1-benzyl ester (29.6 g, 120 mmol) in DMF (250 mL) were added cesium carbonate (42.9 g, 132 mmol) followed by benzyl bromide (17.09 mL, 144 mmol) and sodium iodide (2.15 g, 14.37 mmol) and the mixture was stirred at RT for 48 h. The reaction mixture was quenched with water (500 mL) and extracted with EtOAc (3×200 mL). The organic extracts were combined and washed with brine, dried (Na2SO4), filtered and concentrated. The crude residue was purified by flash column chromatography on silica gel (c-hexane/EtOAc 4:1) to give the desired material. MS (UPLC/MS): 338 [MH-Boc]+; tR (HPLC conditions b): 2.31 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09388199B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-b35c9226983948cfa02c054a65a95f7e |
| Source note | uspto-grants-2016_07 |