HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → (R)-4-[(1-Methyl-2,2,2-trifluoro-ethylamino)-methyl]-benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-Cyanobenzaldehyde | HCID 66042 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | (2R)-1,1,1-Trifluoropropan-2-amine--hydrogen chloride (1/1) | HCID 44593757 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (R)-4-[(1-Methyl-2,2,2-trifluoro-ethylamino)-methyl]-benzonitrile | HCID 59828823 | 27.2% |
Reaction Steps
Add sodium cyanoborohydride (3.36 g, 53.5 mmol) to a solution of 4-cyanobenzaldehyde (1.75 g, 13.35 mmol) and (R)-1-methyl-2,2,2-trifluoro-ethylamine hydrochloride (2 g, 13.37 mmol) in methanol (17 mL) containing acetic acid (1.53 mL, 26.75 mmol). Stir the mixture at room temperature overnight. Partition the mixture between 1N aqueous NaOH/DCM (1:1, 500 mL) and extract the aqueous layer twice with DCM. Dry the combined organic extracts over MgSO4, concentrate in vacuo and purify by chromatography on silica gel (120 g) eluting with hexane/EtOAc (19:1, 9:1, 85:15 and 4:1) to obtain the desired intermediate (0.83 g, 27%). MS (ES+) m/z: 229 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08680091B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-e6d71cbd1e324fadb2d0c77c10a71133 |
| Source note | uspto-grants-2014_03 |