Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethylene | HCID 6325 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1-Butene | HCID 7844 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-butyl trifluoroacetate | HCID 244758 | — |
Reaction Steps
In addition, the esterification of olefins with carboxylic acids and subsequent ester hydrolysis of the alkyl esters formed to the corresponding alcohol with recovery of the acid is known. For instance, U.S. Pat. No. 4,384,148 describes the reaction of ethene with acetic acid to give ethyl acetate in an autoclave. The subsequent hydrolysis of the ethyl acetate removed by distillation with water in a molar ratio of 1:5 in an autoclave affords a mixture comprising ethyl acetate, ethanol and diethyl ether. GB 2 238 539 discloses the two-stage hydration of 1-butene by reaction with trifluoroacetic acid to give 2-butyl trifluoroacetate in the presence of a highly acidic ion exchange resin and subsequent hydrolysis of the ester to give 2-butanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07750194B2 |
|---|
| Source dataset | uspto-grants-2010_07 |
|---|
| ORD ID | ord-4794efa700334bfbb378f61837898ac7 |
|---|
| Source note | uspto-grants-2010_07 |
|---|