HuagongsheHuagongshe Chemistry Print Report · For research reference only
4,4,4-Trifluoro-3-hydroxy-3-methylbutanoic acid → 3-(Trifluoromethyl)-3-hydroxybutyric acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4,4,4-Trifluoro-3-hydroxy-3-methylbutanoic acid | HCID 136168 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(Trifluoromethyl)-3-hydroxybutyric acid methyl ester | HCID 85646493 | 100% |
Reaction Steps
To a solution of 4,4,4-trifluoro-3-hydroxy-3-methylbutyric acid (1.81 g, 10.0 mmol) in methanol (10 ml) was added (trimethylsilyl)diazomethane (10 ml), dropwise. The reaction was then stirred at room temperature for 4 h. Removal of the solvent afforded the crude 3-(trifluoromethyl)-3-hydroxybutyric acid methyl ester as a yellow oil (1.92 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07671080B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-263381dfbe584384bb7f02dbf1c5b9aa |
| Source note | uspto-grants-2010_03 |