HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → (R)-2-amino-3-methyl-N-(2,2,2-trifluoroethyl)butanamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | (R)-tert-butyl 3-methyl-1-oxo-1-(2,2,2-trifluoroethylamino)butan-2-ylcarbamate | HCID 117628462 | — |
| Product | (R)-2-amino-3-methyl-N-(2,2,2-trifluoroethyl)butanamide hydrochloride | HCID 117628603 | — |
Reaction Steps
(R)-tert-butyl 3-methyl-1-oxo-1-(2,2,2-trifluoroethylamino)butan-2-ylcarbamate I-3a (12.81 g, 42.9 mmol) was dissolved in DCM (30 ml), and TFA (12 ml, 156 mmol) slowly added. The reaction was allowed to stir at room temperature for 2 hr. The mixture was concentrated in vacuo to an oil. The oil was dissolved in DCM and washed with aq. sodium bicarbonate (50 mL) dried over sodium sulfate, filtered and concentrated to an oil. The oil was dissolved in ethyl acetate, cooled to 0° C. and treated with 1N HCL in diethyl ethere to give upon filtration 10.0 gm solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09096598B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-ba2873096b3b4172ba1fd7e2af234aeb |
| Source note | uspto-grants-2015_08 |