HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 14795882, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl 4-(tributylstannyl)benzoate | HCID 13256035 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 14795882 | HCID 14795882 | 90.3% |
Reaction Steps
To a solution of methyl 4-tri-n-butylstannylbenzoate (3.0 g, 7 mmol) in absolute ethanol (60 ml) was added 0.25 g KOH (9 mmol). The resulting solution was refluxed for 2 hours. The solution was cooled and poured into an ice-cold solution of acetic acid (0.64 g, 10.6 mmol) and water (100 ml). The solution was then extracted with diethyl ether (80 ml). The ether phase was washed with water (30 ml), dried over MgSO4 (5 g), filtered and evaporated under reduced pressure to afford 2.6 g (88%) of the title compound. This material was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05746997 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-871560983abd480daa5fe2479ef7f7f5 |
| Source note | uspto-grants-1998_05 |