HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Phenyl[3-(4-fluoro-2-nitrophenoxy)propyl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 3-(4-Fluoro-2-nitrophenoxy)propylamine | HCID 62348405 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Phenyl[3-(4-fluoro-2-nitrophenoxy)propyl]carbamate | HCID 86641934 | 94.2% |
Reaction Steps
Triethylamine (2.90 ml, 21.4 mmol) and phenyl chlorocarbonate (2.52 ml, 20.0 mmol) were added to a dioxane solution (43 ml) of 3-(4-fluoro-2-nitrophenoxy)propylamine (4.03 g, 18.8 mmol), while being cooled with ice, and the mixture was stirred at room temperature for 0.5 hours. The reaction mixture was concentrated under reduced pressure, and the residue was then purified by silica gel column chromatography (dichloromethane:ethyl acetate=30:1). The purified product was concentrated to dryness under reduced pressure to thereby obtain 5.92 g of powdery yellow phenyl[3-(4-fluoro-2-nitrophenoxy)propyl]carbamate (yield: 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642619B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-ec5108af1df542c88c0e0d3b2918c4fe |
| Source note | uspto-grants-2014_02 |