HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2'-Bipyridine → Ethyl N-(2-ethoxyphenyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2'-Bipyridine | HCID 1474 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Carbamic acid, (2-bromophenyl)-, ethyl ester | HCID 4182114 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethyl N-(2-ethoxyphenyl)carbamate | HCID 307457 | 84% |
Reaction Steps
2.44 g of the 2-bromo-1-ethoxycarbonylaminobenzene was added to a solution containing 680 mg of sodium ethoxide, 170 mg of cupric chloride dihydrate, and 156 mg of 2,2'-bipyridine in 40 ml of methanol, and the mixture was heated under reflux for 1.5 hours. After the temperature was brought to room temperature, ethyl acetate was added thereto, and the resulting mixture was washed with water and dried over Glauber's salt. The solvent was distilled off, and the obtained crude crystals were recrystallized from a n-hexane/ethyl acetate solvent mixture, to obtain 1.75 g (yield: 84%) of the desired compound. The spectrum data of the compound was in agreement with the spectrum data of the separately synthesized reference compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05006660 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-1e988eddc57242e286eaddb6360593da |
| Source note | uspto-grants-1991_04 |