HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Bromide → 2-Isobutyl-succinic acid-4-t-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | 2-Isobutylsuccinic acid-4-t-butyl ester-1-methyl ester | HCID 21888314 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-Isobutyl-succinic acid-4-t-butyl ester | HCID 9942712 | 95.4% |
Reaction Steps
Anhydrous lithium bromide (10.6 g, 121.8 mmol) was added to a stirring mixture of 2 (5.95 g, 24.4 mmol) in acetone (50 mL) under argon, and the mixture was refluxed for 2 hours. After cooling, the acetone was evaporated under reduced pressure, and the residue was taken up in ether (50 mL), washed with water (50 mL), brine, dried (MgSO4), and the solvent was evaporated under reduced pressure. The residue was chromatographed (SiO2, heptane/ethyl acetate, 95:5) to give the dibromide 3 (5.36 g, 86%) as an orange liquid; Rf(heptane-ethyl acetate, 8:2), 0.82. δH (400 MHz; CDCl3): 3.6 (2H, m), 3.45 (2H, m), 2.85 (2H, m), 2.1 (2H, m), 1.7 (2H, m; δc(400 MHz; CDCl3): 39.70, 33.79, 23.95.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07189747B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-37b02f9e5de84c629a758513b289c411 |
| Source note | uspto-grants-2007_03 |