Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 90415324 | HCID 90415324 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 90413589 | HCID 90413589 | 30% |
Reaction Steps
2,2,4,6-Tetrafluorobenzo[d][1,3]dioxole (500 mg, 2.6 mmol) was dissolved in dry tetrahydrofuran (7 mL), cooled to −70° C., treated dropwise with sec-BuLi (1.3 M; 2.1 mL, 2.7 mmol) and stirred for 1 h at −70° C. This mixture was treated dropwise with a solution of iodine (1.1 g, 4.4 mmol) in tetrahydrofuran (5 mL) over 10 min. After 2 h at −70° C., the mixture was treated with saturated NH4Cl, extracted with ethyl ether, dried (Na2SO4) and evaporated. The material was purified by reverse phase HPLC with 85% acetonitrile-water to give the title compound (250 mg; 30%): 1H NMR (400 MHz, CDCl3) δ 6.80-6.77 (d, J=8.7 Hz, 1H), 6.77-6.75 (d, J=8.7 Hz, 1H); 19F NMR (376 MHz, CDCl3) δ −48.72, −99.73, −132.62; EIMS m/z 320.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09149038B2 |
|---|
| Source dataset | uspto-grants-2015_10 |
|---|
| ORD ID | ord-34650789ee5240d890681197cb1929cd |
|---|
| Source note | uspto-grants-2015_10 |
|---|