HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 12449510, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 12449500 | HCID 12449500 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12449510 | HCID 12449510 | — |
Reaction Steps
A solution of 52.3 g. of α-(α,α,α-trifluoro-p-tolyl)-4-morpholineacetonitrile in 500 ml. of dry tetrahydrofuran is stirred at ambient temperature while 1 ml. portions of 30% potassium hydroxide in ethanol and 25 ml. portions of ethyl acrylate is added every half hour until a total of 5 ml. of the base and 150 ml. of ethyl acrylate is added. After the addition, the mixture is stirred at ambient temperature for 48 hours. Following filtration, the filtrate is concentrated, dissolved in methylene chloride, passed through magnesol and recrystallized from methylene chloride/hexane to afford ethyl γ-cyano-γ(α,α,α-trifluoro-p-tolyl)-4-morpholinebutyrate as cream colored crystals, m.p. 96° -97° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04112095 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-556ce4f2e1c741ada993ba0bfd9ca199 |
| Source note | uspto-grants-1978_09 |