HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 44252387, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 4-benzyl-4-((dimethylamino)methyl)-N-methyl-1-phenylcyclohexanamine | HCID 68632271 | — |
| Reactant | CID 101953985 | HCID 101953985 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 44252387 | HCID 44252387 | — |
Reaction Steps
A solution of the title compound from Example 33 (1.40 g, 4.16 mmol) and formalin (5.8 mL, 37% aqueous solution) in acetonitrile (40 mL) was mixed in portions with sodium cyanoboron hydride (1.03 g, 16.6 mmol) and stirred for 45 min at room temperature. Concentrated acetic acid was then added until a neutral reaction occurred and the mixture stirred for 45 min at room temperature. For work up the solvent was removed in a vacuum, the residue taken up in 2N NaOH (40 mL) and then extracted with ether (3×40 mL). The organic phase was dried over Na2SO4, filtered and concentrated to low volume in a vacuum. The remaining residue was purified by flash chromatography with ethyl acetate (methanol→methanol+2% TEA).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08835689B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-ac0487d09f5244bd95753c00e131cd7c |
| Source note | uspto-grants-2014_09 |