HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 3-Iodo-5-(4-trifluoromethylphenyl)indole-2-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | Ethyl 5-(4-(trifluoromethyl)phenyl)-1H-indole-2-carboxylate | HCID 57419913 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-Iodo-5-(4-trifluoromethylphenyl)indole-2-carboxylic acid ethyl ester | HCID 57419914 | — |
Reaction Steps
NaI (2.04 g, 14 mmol) in acetone (10 mL) was added dropwise to a stirred solution of N-chlorosuccinimide (1.83 g, 14 mmol) in acetone (10 mL) protected from light. After 15 min, a solution of 5-(4-trifluoromethylphenyl)indole-2-carboxylic acid ethyl ester (3.80 g, 11 mmol; see step (a) above) in acetone (60 mL) was added dropwise, followed by stirring for 2 h at rt. The mixture was poured into Na2S2O3 (aq, 10%, 250 mL) and extracted with EtOAc (200 mL). The combined extracts were washed with NaHCO3 (aq, sat), water and brine, dried (Na2SO4) and concentrated. The residue was treated with petroleum ether to give the sub-title compound. Yield 4.88 g (93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08097623B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-2726ce31a1a94c6d992276d562473f9f |
| Source note | uspto-grants-2012_01 |