HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Methyl 2-heptyloxy-4-iodobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-Iodoheptane | HCID 20274 | — |
| Reactant | Methyl 4-iodosalicylate | HCID 11380407 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-heptyloxy-4-iodobenzoate | HCID 68767792 | 100% |
Reaction Steps
A suspension of caesium carbonate (35.2 g, 108 mmol), methyl 4-iodo-2-hydroxybenzoate (25 g, 90 mmol), iodoheptane (19.2 ml, 117 mmol) in DMF (500 ml) is stirred for 10 hours at room temperature. The organic phase is acidified at room temperature with a 2N hydrochloric acid solution to pH 5. The desired product is extracted by addition of ethyl acetate. The organic phase is washed with water, dried with magnesium sulfate and concentrated using a rotary evaporator. After evaporation of the remainder of the iodoheptane by placing the oil obtained under vacuum produced by a rotary vane pump, 33.8 g (100%) of the expected compound are recovered in the form of a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07829588B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-0e218b050248476fb30901644d11cf9b |
| Source note | uspto-grants-2010_11 |