HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → Ethyl 1-(phenylaminocarbonyl)cyclopropanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 1-(Ethoxycarbonyl)cyclopropanecarboxylic acid | HCID 11789472 | — |
| Reactant | Ethyl 1-(4-chloro-2-ethylphenylaminocarbonyl)cyclopropanecarboxylate | HCID 19096849 | — |
| Product | Ethyl 1-(phenylaminocarbonyl)cyclopropanecarboxylate | HCID 14150218 | — |
Reaction Steps
1-Carboethoxycyclopropanecarboxylic acid (3.95 grams, 0.025 mole), ethyl chloroformate (2.71 grams, 0.025 mole) and aniline (2.33 grams, 0.025 mole) were reacted sequentially in the presence of triethylamine (2.53 grams, 0.025 mole) in a manner similar to that described for ethyl 1-(4-chloro-2-ethylphenylaminocarbonyl)cyclopropanecarboxylate in Example XXXIII to give ethyl 1-(phenylaminocarbonyl)cyclopropanecarboxylate which was then hydrolyzed in a manner similar to that described in Example VII to give 2.42 grams (0.01 mole) of 1-(phenylaminocarbonyl)cyclopropanecarboxylic acid having a melting point of 178° C.-181° C. NMR analysis of the product indicated the following:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05123951 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-2cda3b49a0244928a99782c62d43e892 |
| Source note | uspto-grants-1992_06 |