HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminobiphenyl → ethyl N-biphenyl-2-yloxamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminobiphenyl | HCID 7015 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethoxalyl chloride | HCID 20884 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | ethyl N-biphenyl-2-yloxamate | HCID 311876 | 85% |
Reaction Steps
5.08 g (30 mmol) of 2-aminobiphenyl, 50 ml of ethyl acetate, and 3.1 g (30 mmol) of triethylamine were placed in a flask, to which 4.1 g (30 mmol) of ethyl chloroglyoxylate was added dropwise under ice cooling. The reaction mixture was stirred at room temperature for three hours, and then 50 ml of ethyl acetate was added thereto. The organic layer was washed with 30 ml of 1N hydrochloric acid and 30 ml of brine one by one, and then was dried with anhydrous sodium sulfate. The solvent was removed by evaporation to obtain 6.8 g (24 mmol, yield 85%) of ethyl N-biphenyl-2-yloxamate as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08258302B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-c50bfdd9cd174583b5a5e42ddf0d3cee |
| Source note | uspto-grants-2012_09 |