HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetonitrile → HCID 86052719, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenyl(piperidin-4-ylidene)acetonitrile | HCID 59681564 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86052719 | HCID 86052719 | 21.2% |
Reaction Steps
To a solution of 2-phenyl-2-(piperidin-4-ylidene)acetonitrile (6.8 g, 34 mmol) in THF (150 mL) was added NEt3 (40 mL, 300 mmol) and chloroacetonitrile (20 mL, 315 mmol) and the reaction was stirred 16 h. The precipitates was filtered away and the filtrate concentrated to dryness. The residues was purified by silica gel chromatography (Biotage 40-short, 20% EtOAc/Hex to 50% EtOAc/Hex) to yield 42 (1.7 g, 7.2 mmol, 21%) as a yellow waxy solid. 1H NMR: (500 MHz, CDCl3) δ 7.44-7.34 (m, 3H), 7.30-7.27 (m, 2H), 3.65 (s, 2H), 2.96 (t, J=5.3 Hz, 2H), 2.90 (t, J=5.3 Hz, 2H), 2.70 (t, J=5.6 Hz, 2H), 2.62 (t, J=5.6 Hz, 2H); LC/MS: (ES+) m/z (M+H)+=238; HPLC Rt=1.33 min., column 0, conditions B.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07902204B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-d9d9ca67164b46ceb59441fb69d9f12d |
| Source note | uspto-grants-2011_03 |