HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 57625337, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-Fluorobenzylamine | HCID 67326 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 1-(Trifluoroacetyl)piperidin-4-one | HCID 15080943 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57625337 | HCID 57625337 | 37% |
Reaction Steps
4-Fluorobenzylamine (3.14 g, 25.9 mmol) was dissolved in methanol (150 mL). 1-(trifluoroacetyl)-4-piperidone (5.07 g, 25.9 mmol) was added, and the pH was adjusted to ˜5 with acetic acid. The reaction mixture was stirred for 5 min and NaBH3CN (2.46 g, 38.9 mmol) was added slowly under stirring. After 20 h at room temperature the reaction was concentrated. 2 M NaOH (100 mL) was added and the aqueous phase was extracted with dichloromethane (2×100 mL). The combined organic phases were dried over Na2SO4, filtered and concentrated to give N-(4-fluorobenzyl)-1-(trifluoroacetyl)piperidin-4-amine (50ELH85, 2.91 g, 37%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538222B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-e05127306548415d8e3a5fa7d3f4599e |
| Source note | uspto-grants-2009_05 |