HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopentanone → Methyl 3-(cyclopentylamino)-2,2-difluoropropanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopentanone | HCID 8452 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 22635306 | HCID 22635306 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 3-(cyclopentylamino)-2,2-difluoropropanoate | HCID 67117821 | 60% |
Reaction Steps
To a round bottom flask was added methyl 3-amino-2,2-difluoropropanoate (570 mg, 3.24 mmol), THF (20 mL), cyclopentanone (0.433 mL, 4.87 mmol), and HOAc (1 mL). To this mixture was added sodium triacetoxyborohydride (1.06 g, 5 mmol) portionwise. The reaction was left to stir overnight. It was then added slowly to a stirring solution of ice, NaHCO3 (sat.), and EtOAc. The aqueous layer was further extracted with EtOAc, the organic extracts combined, dried over MgSO4, filtered and concentrated to yield the desired product as clear syrup (400 mg, 60%). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.30 (td, J=13, 6 Hz, 2H) 1.43 (d, J=8 Hz, 1H) 1.47-1.70 (m, 4H) 1.77 (dt, J=12, 6 Hz, 2H) 3.12 (t, J=6 Hz, 1H) 3.19 (t, J=14 Hz, 2H) 3.88 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08026234B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-96143d9f98414f43a7d9eda56ffc2a7d |
| Source note | uspto-grants-2011_09 |