HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Acetate → Diethyl-2,5-bis-(6-acetoxyhexoxy)terephthalate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Diethyl-2,5-bis-(6-bromohexoxy)terephthalate | HCID 19354089 | — |
| Catalyst | Trioctylmethylammonium chloride | HCID 21218 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Diethyl-2,5-bis-(6-acetoxyhexoxy)terephthalate | HCID 19354093 | — |
Reaction Steps
50.0 g (86.0 mmol) diethyl-2,5-bis-(6-bromohexoxy)terephthalate, 84.5 g (861 mmol) potassium acetate and 4.4 g (11 mmol) methyl trioctyl ammonium chloride (Aliquat 336®, tricaprylyl methyl ammonium chloride, Fluka, CAS 5137.55.3) in 500 ml absolute acetonitrile are heated under reflux in a nitrogen atmosphere for 48 hours. After distilling off the solvent, the reaction mixture is taken up in 1200 ml ethyl acetate and washed three times with water (3×300 ml). The organic phase is dried over MgSO4 and the solvent is then distilled off. 1000 ml petroleum ether is added to the residual, oily residue and the product crystallizing out after 16 hours at -20° C. is recrystallized from petroleum ether/ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06031015 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-139807bff8214104b3c511448b127cac |
| Source note | uspto-grants-2000_02 |