HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → Trifluoroacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Phenothiazine | HCID 7108 | — |
| Reactant | Acrylonitrile | HCID 7855 | — |
| Product | Trifluoroacetic acid | HCID 6422 | — |
| Product | Acrylonitrile | HCID 7855 | — |
| Product | tert-Butylacrylamide | HCID 7877 | — |
Reaction Steps
84 g of acrylonitrile are added dropwise to a solution of 1 g of phenothiazine in 90 g of trifluoroacetic acid at 20° C., whilst stirring. Thereafter, 43 g of tert.-butanol are added dropwise at 35° C. The reaction mixture is kept at 60° to 70° C. for 6 hours and then worked up by distillation. Acrylonitrile, trifluoroacetic acid and some of the N-tert.-butylacrylamide formed are distilled off under reduced pressure. 36 g of N-tert.-butylacrylamide (melting point 120° to 122° C.) remain as the distillation bottom product. The distillate can be re-used in the reaction with the same result.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04246199 |
| Source dataset | uspto-grants-1981_01 |
| ORD ID | ord-c3e7a1b1f2b24d75a824b165907cc7af |
| Source note | uspto-grants-1981_01 |