HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalic Acid → 2-(Trimethylsilyl)ethyl 2-(2-iodophenyl)butanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalic Acid | HCID 971 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2-(Trimethylsilyl)ethanol | HCID 18013 | — |
| Reactant | 2-(2-Iodophenyl)butanoic acid | HCID 22456433 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(Trimethylsilyl)ethyl 2-(2-iodophenyl)butanoate | HCID 53967596 | 78.4% |
Reaction Steps
To a solution of the acid of Step 1 (103 g, 0.356 mol), pyridine (58 mL, 0.717 mol) and 2-(trimethylsilyl)ethanol (61.2 mL, 0.427 mol) in CH3CN (270 mL) was added a solution of dicyclohexylcarbodiimide (73.4 g, 0.356 mol) in CH3CN (100 mL). The reaction mixture was stirred at r.t. for 2 h, at which point 5M oxalic acid in DMF solution (11 mL) was added. After stirring for 30 min, the suspension was filtered and the filtrate was diluted with EtOAc, washed with water and dried over MgSO4. The crude product was distilled under reduced pressure to give 109 g of the title compound as a colorless oil (bp 120°-140° C./0.4 mm Hg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05565473 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-94039dd6958444f1a8cbfcea078d9d5d |
| Source note | uspto-grants-1996_10 |