HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → Benzyl (2,4-difluorophenyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2,4-Difluoroaniline | HCID 9709 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl (2,4-difluorophenyl)carbamate | HCID 11954520 | 85% |
Reaction Steps
To 2,4-difluoro-phenylamine (30, 7.0 mL, 70.0 mmol) in 100 mL of dichloromethane, pyridine (11 mL, 0.14 mol) and benzyl chloroformate (31, 11.9 mL, 83.4 mmol) are added. The reaction mixture is stirred at ambient temperature for 1.5 hours. The reaction mixture is concentrated under vacuum and the residue is partitioned between ethyl acetate and potassium bisulfate solution. The organic layer is dried with magnesium sulfate, filtered, and the filtrate concentrated under vacuum. The resulting material is crystallized from hexanes to provide the desired compound (32, 15.6 g, 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08673928B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-7b50e0b8e6ee4460a6de76c0dd33449b |
| Source note | uspto-grants-2014_03 |