HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 3-Amino-5-ethoxy-4-iodo-benzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | Methyl 3-amino-5-hydroxy-4-iodobenzoate | HCID 68458438 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Amino-5-ethoxy-4-iodo-benzoic acid methyl ester | HCID 68459579 | 69.6% |
Reaction Steps
To a solution of 3-amino-5-hydroxy-4-iodo-benzoic acid methyl ester (0.25 g, 0.85 mmol) in DMF (3 mL) and ethyl iodide (0.10 mL, 0.146 g, 0.94 mmol) at 0° C. was added sodium tert-butoxide (0.11 g, 0.94 mmol) in small portions over a time period of 10 min. After stirring for 1 h, the cooling bath was removed and the reaction mixture stirred at rt for an additional 18 h. The solution was concentrated by evaporation under reduced pressure and extracted with ethyl acetate (3×50 mL). The combined organic phases were dried over MgSO4, concentrated by evaporation under reduced pressure and the crude material purified with column chromatography on silica eluting with hexane/ethyl acetate (2:1) yielding 0.19 g (69%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07772253B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-ea048377ca0c478596b80b4e3e8e8be2 |
| Source note | uspto-grants-2010_08 |