HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → HCID 58841176, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 18448167 | HCID 18448167 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58841176 | HCID 58841176 | — |
Reaction Steps
A solution of 5 mmol of (2Z)-4-{[(4-bromobutoxy)carbonyl]oxy}-3-[4-(methylsulfonyl)phenyl]-2-phenylbut-2-enoic acid with 3 mL of EtI in 30 mL of DMF was stirred with 5 mmol of K2CO3 at rt for 30 min. The reaction was quenched with sat. NH4Cl/H2O, extracted with EtOAc, Dried over Na2SO4, evaporated, and purified by flash chromatography (5–50% EtOAc/hexane) to afford 2.7 g of the titled compound. 1H NMR (acetone-d6, 500 MHz): δ 7.80 (d, 2 H), 7.48 (d, 2 H), 7.22–7.17 (m, 3 H), 7.15–7.08 (m, 2 H), 5.30 (s, 2 H), 4.32 (m, 4 H), 3.54 (t, 2 H), 3.12 (s, 3 H), 1.95–1.84 (m, 2 H), 1.83–1.70 (m, 2 H) 1.31 (t, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07199154B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-f4f1fe244e264e5f958d8c059dc5090a |
| Source note | uspto-grants-2007_04 |