HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → HCID 12051933, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 12051932 | HCID 12051932 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 12051933 | HCID 12051933 | — |
Reaction Steps
The title compound from Example 1 (0.30 g) was dissolved in dry DMF (10 mL) and added NaH (62 mg; 60% in oil) at room temperature under a nitrogen atmosphere. The reaction mixture was stirred for 5 mins., and then added EtI (0.2 mL) and continued for an additional 24 h. The reaction mixture was partitioned between ethyl acetate (25 mL) and water (25 mL), washed the organic layer with brine, dried, and stripped in vacuum to yield a pale yellow oil. The sample was purified by flash column chromatography (1:100 MeOH +CH2Cl2) to afford the title compound as a colorlesss oil (0.16 g). Elemental analysis for C19H25BrN6 : Theory C: 54.68, H: 6.05 Found: C: 54.66, H: 6.02.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06107300 |
| Source dataset | uspto-grants-2000_08 |
| ORD ID | ord-b22e2d18eb104585960101487f34cc7f |
| Source note | uspto-grants-2000_08 |