HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Methyl [2-(2-chloro-4-fluoro-5-methoxycarbonylaminophenoxy)phenoxy]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Methyl [2-(5-amino-2-chloro-4-fluorophenoxy)phenoxy]acetate | HCID 23380315 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Methyl [2-(2-chloro-4-fluoro-5-methoxycarbonylaminophenoxy)phenoxy]acetate | HCID 86584265 | — |
Reaction Steps
Into a mixture of methyl [2-(5-amino-2-chloro-4-fluorophenoxy)phenoxy]acetate [Intermediate compound A3-22], methyl chloroformate and tetrahydrofuran is added dropwise pyridine, and the mixture is stirred at room temperature. Dilute hydrochloric acid is added to the reaction solution, and this is extracted with ethyl acetate. The organic layer is washed with saturated saline, dried over anhydrous magnesium sulfate, and concentrated to obtain methyl [2-(2-chloro-4-fluoro-5-methoxycarbonylaminophenoxy)phenoxy]acetate [Intermediate compound A9-22].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06667413B2 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-ef274cf11d504a32a54c037f5fc9dbdb |
| Source note | uspto-grants-2003_12 |