HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 59264605, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-(4-TRIFLUOROMETHYLPHENYL)BENZYLAMINE | HCID 3729155 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 59264611 | HCID 59264611 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59264605 | HCID 59264605 | 57.5% |
Reaction Steps
A mixture of 1,1-dimethylethyl 2-methyl-2-(4-oxo-1-piperidinyl)propanoate (Int. A6) (370 mg, 1.2 equiv), {[4′-(trifluoromethyl)-4-biphenylyl]methyl}amine (Int. A1) (397 mg, 1 equiv), sodium triacetoxyborohydride (400 mg, 1.5 equiv), DCM (10 ml) and acetic acid (0.076 ml, 1 equiv) was combined and stirred at room temperature until LCMS confirmed disappearance of the amine starting material (approx. 18 hours). Aqueous sodium carbonate was added and then extracted with DCM. The organics were dried over sodium sulfate and concentrated to give a solid (420 mg) that was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07705005B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-6c3f25d81db145a0bc3b9263580fb6a4 |
| Source note | uspto-grants-2010_04 |