Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-Methylformamide | HCID 31254 | — |
| Reactant | HCID 131728373 | HCID 131728373 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 57526215 | HCID 57526215 | 71% |
Reaction Steps
A mixture of CF3OCF2CF2CH2CH2I, (92 g, 0.27 mol) and N-methyl-formamide (119 mL), was heated to 150° C. for 26 hours. Then the reaction was cooled to 100° C., followed by the addition of water to separate the crude ester. Ethyl alcohol (30 mL) and p-toluene sulfonic acid (1.03 g) were added to the crude ester, and the reaction was stirred at 70° C. for 15 minutes. Then ethyl formate and ethyl alcohol were distilled out to give a crude product. The crude product was dissolved in ether, washed with aqueous sodium sulfite, water, and brine in turn, then dried over magnesium sulfate. The product was then distilled to give 44 g of CF3OCF2CF2CH2CH2OH in 71% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07815816B2 |
|---|
| Source dataset | uspto-grants-2010_10 |
|---|
| ORD ID | ord-ad2bf96bb0784d4ba8a8501dc247077e |
|---|
| Source note | uspto-grants-2010_10 |
|---|