HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 2-(2-Iodophenyl)butanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 2-Iodophenylacetic acid | HCID 2780090 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-Iodophenyl)butanoic acid | HCID 22456433 | 75.3% |
Reaction Steps
To a solution of diisopropylamine (5.6 mL, 40 mmol) in dry THF (60 mL) at -10° C. was added 1.6M BuLi (25 mL, 40 mmol). After 30 min, a solution of 2-iodophenylacetic acid (5.24 g, 20 mmol) in THF (20 mL) was slowly added. The solution was stirred for 1 h, at which point iodoethane (1.6 mL, 117 mmol) was added. After 2 h at r.t. the reaction was quenched with 0.5M NH4OAc solution and 6M HCl (10mL) and the product was extracted with EtOAc. The organic layer was dried (MgSO4) and evaporated to give an oily residue which was purified by flash chromatography (15:85 EtOAc:hexane containing 5% AcOH) to give 4.37 g of the title compound as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05270324 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-bfe47c8dca4d4257a22b46c888d1a9ae |
| Source note | uspto-grants-1993_12 |