HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → Phenyl N-(3-chloropropyl)-N-(2,2,2-trifluoroethyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | (3-Chloropropyl)(2,2,2-trifluoroethyl)amine | HCID 65027041 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Phenyl N-(3-chloropropyl)-N-(2,2,2-trifluoroethyl)carbamate | HCID 118046857 | — |
Reaction Steps
Into a 500-mL round-bottom flask, was placed (3-chloropropyl)(2,2,2-trifluoroethyl)amine (5 g, 28.48 mmol, 1.00 equiv), dichloromethane (300 mL), TEA (5.8 g, 57.32 mmol, 2.00 equiv), pyridine (0.5 mL). To this was added dropwise phenyl chloroformate (4.4 g, 28.10 mmol, 1.00 equiv) at 0° C. The resulting solution was stirred for 3 h at room temperature. The resulting mixture was washed with 2×100 mL of H2O. The resulting mixture was washed with 2×100 mL of brine. The mixture was dried over sodium sulfate. The resulting mixture was concentrated under vacuum. This resulted in 1.4 g (crude) of phenyl N-(3-chloropropyl)-N-(2,2,2-trifluoroethyl)carbamate as a colorless liquide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447084B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-d88794e752b94b8592b3cde2735736e0 |
| Source note | uspto-grants-2016_09 |