HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 23160669, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 15421643 | HCID 15421643 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23160669 | HCID 23160669 | 15% |
Reaction Steps
1-[4-(Trifluoromethyl)phenyl]azetidin-2-one (2.3 g, 10.7 mmol) was dissolved in 1,2-dichloroethane (20 mL), trifluoromethanesulfonic acid (1 mL) was added at 0° C., and the mixture was stirred at room temperature for 30 min. Triethylamine (2.2 mL) was added to the reaction mixture, and the mixture was worked-up according to a conventional method to give a crude product. The obtained crude product was dissolved in ethanol (10 mL), sodium borohydride (0.81 g, 21.4 mmol) was added, and the mixture was stirred for 4 hrs. The solvent was evaporated and the residue was purified by silica gel column chromatography to give the title compound (0.35 g, 1.6 mmol, 15%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879863B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-25014553b19c40bc9435840abef1e382 |
| Source note | uspto-grants-2011_02 |