HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Acetate → Tert-butyl 2-amino-2-(3-fluorophenyl)ethylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | tert-butyl N-[2-(3-fluorophenyl)-2-oxoethyl]carbamate | HCID 84173790 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Tert-butyl 2-amino-2-(3-fluorophenyl)ethylcarbamate | HCID 76853774 | 94% |
Reaction Steps
To a flask were added tert-butyl[2-(3-fluorophenyl)-2-oxoethyl]carbamate (0.32 g, 1.3 mmol) and ammonium acetate (2.02 g, 26.2 mmol) and methanol (10 mL) and sodium cyanoborohydride (0.22 g, 3.5 mmol). The mixture was refluxed for 2 h. The solvent was removed under vacuum. To the residue was added EtOAc and 50 mL of 1M NaOH. The aqueous phase was extracted again with fresh EtOAc. The combined organic extracts were dried over sodium sulfate, filtered and dried under vacuum to give 0.301 g (94% yield) of the final product as oil. LC-MS found: 155.1 (M−Boc)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895571B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-ea277ebecd2a4704bf0fe33706cb0ab8 |
| Source note | uspto-grants-2014_11 |