HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoromethanesulfonic acid → Methyl (S)-3-benzyloxybutyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | Benzyl 2,2,2-trichloroacetimidate | HCID 144968 | — |
| Reactant | Methyl 3-hydroxybutyrate, (S)- | HCID 6950307 | — |
| Solvent | Dichloromethane cyclohexane | HCID 21916607 | — |
| Product | Methyl (S)-3-benzyloxybutyrate | HCID 13967615 | — |
Reaction Steps
Methyl (S)-(+)-3-hydroxybutyrate (17) (2.223 g, 18.82 mmol) and benzyl 2,2,2-trichloroacetimidate (4.2 mL) were dissolved into 37.5 mL of cyclohexane/methylene chloride (2:1). After the addition of 0.2 mL of trifluoromethane sulfonic acid the reaction was stirred under nitrogen for one hour. The reaction was diluted with 75 mL of cyclohexane/methylene chloride (2:1) and filtered. The organic layer was washed with 50 mL of saturated sodium bicarbonate and 50 mL of distilled water. After drying with anhydrous sodium sulfate the solution was filtered and the solvents were removed on a rotovap. The resulting solid was purified using silica gel and elution with ether/hexane (1:4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06306828B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-2dcfd35ef9884360bb841b2fe3e22f0b |
| Source note | uspto-grants-2001_10 |