HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 67071307, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 1-Ethoxy-3-(1-methoxy-1-methylethyl)benzene | HCID 67071555 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67071307 | HCID 67071307 | 110.6% |
Reaction Steps
To a solution of 1-ethoxy-3-(1-methoxy-1-methyl-ethyl)-benzene (5.15 g, 26.51 mmol) in acetonitrile (60 mL) were added N-iodosuccinimide (8.349 g, 37.11 mmol) and trifluoroacetic acid (1.02 mL, 13.26 mmol). The mixture was stirred at room temperature overnight. It was then concentrated in vacuo and the residue was taken in ethyl acetate. After washing with saturated solution of sodium bicarbonate, water and brine, the organic layer was dried over anhydrous sodium sulfate. The solids were filtered off, and the filtrate was concentrated in vacuo to give 9.39 g of 2-ethoxy-1-iodo-4-(1-methoxy-1-methyl-ethyl)-benzene as light brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07851626B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-aea191065e9f4f6995b8a32dd4c7f631 |
| Source note | uspto-grants-2010_12 |