HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylamine → HCID 15868667, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | HCID 15403278 | HCID 15403278 | — |
| Product | HCID 15868667 | HCID 15868667 | 57% |
Reaction Steps
1-(2-Nitrophenyl)-1-ethoxycarbonyl chloride (XIV; R3=H, R4=CH3; 1.4 g; 6 mmol) was dissolved in diisopropylamine (30 ml) under an inert atmosphere and the solution was refluxed for 48 hr. The resulting diisopropylammonium chloride was filtered off and excess of diisopropylamine was removed by evaporation under vacuum to give an oil, which was purified by flash chromatography on silica, eluting with dichloromethane to afford the required compound as a colourless solid. Recrystallization from toluene-petroleum ether (bp 60-80° C.) 2:1 gave colourless crystals (1.0 g; 57% yield), mp 40-41° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06171756B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-5e761aa1caf84bf7a28ee37601ba4ad0 |
| Source note | uspto-grants-2001_01 |