HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Phenylbutyl Isoselenocyanate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | Selenium | HCID 6326970 | — |
| Reactant | Benzyl Isoselenocyanate | HCID 12506035 | — |
| Reactant | Phenylbutyl formamide | HCID 20716133 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Phenylbutyl Isoselenocyanate | HCID 25015746 | 95% |
Reaction Steps
A mixture of phenylbutyl formamide (g, 1.5 mmol), triethylamine (6.4 mmol), 4 Å molecular sieves (g), triphosgene (0.8 mmol), and selenium powder (3.0 mmol) in CH2Cl2 was refluxed and worked up as mentioned for 2a. The crude residue thus obtained was purified by silica gel column chromatography (EtOAc/hexanes 2:98) to give 0.96 g (95%) of 2c as an oil. 1H NMR (CDCl3) δ 1.74-1.76 (m, 4H), 2.66 (t, 2H, J=6.6 Hz), 3.60 (t, 2H, J=5.6 Hz), 7.15-7.32 (m, 5H); HRMS (EI) calcd for C11H13NSe, 239.0208. found, 239.0211.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09126911B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-f67416b9ce9e4dc699447ebe9bfcbf9d |
| Source note | uspto-grants-2015_09 |