HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → ethyl N-(4-chloro-2-fluoro-5-isopropoxyphenyl)-carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Benzenamine, 4-chloro-2-fluoro-5-(1-methylethoxy)- | HCID 158649 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl N-(4-chloro-2-fluoro-5-isopropoxyphenyl)-carbamate | HCID 20026143 | — |
Reaction Steps
12.8 g of ethyl chloroformate are added while stirring to a solution of 20 g of 4-chloro-2-fluoro-5-isopropoxyaniline in 100 ml of methylene chloride at room temperature. 9.4 g of pyridine are subsequently added dropwise during 20 minutes at 20° C. while stirring and cooling. The reaction mixture is stirred for 20 minutes, washed three times with in each case 200 ml of a solution of 20 ml of 2N hydrochloric acid in 200 ml of water, dried over anhydrous sodium sulphate and evaporated to dryness under reduced pressure. There is obtained ethyl N-(4-chloro-2-fluoro-5-isopropoxyphenyl)-carbamate, m.p. 89°-91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04859229 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-bd4e217845554cfe96ccae5c5490f16d |
| Source note | uspto-grants-1989_08 |