Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diphosgene | HCID 10426 | — |
| Reactant | 4-Chloro-2-fluoroaniline | HCID 93898 | — |
| Reactant | Glycine ethyl ester, hydrochloride | HCID 2723640 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | HCID 86743764 | HCID 86743764 | — |
Reaction Steps
To a stirred solution of 20.0 g (0.137 mole) of 4-chloro-2-fluoroaniline in 300 mL of toluene was slowly added 16.2 g (0.082 mole) of trichloromethyl chloroformate. The reaction mixture was heated at reflux for approximately 18 hours. The mixture was cooled, and the solvent was removed by distillation under reduced pressure leaving an oil. The oil was dissolved in 100 mL of chloroform, and 20.6 g (0.15 mole) of glycine ethyl ester hydrochloride was added. Triethylamine (15.2 g, 0.15 mole) was added slowly, and the resultant mixture was stirred at room temperature for two hours. The reaction mixture was diluted with 300 mL of n-heptane and 100 mL of water, causing a precipitate to form. The precipitate was collected by filtration to give 36.4 g of ethyl 4-chloro-2-fluorophenylaminocarbonylaminoacetate, m.p. 125°-129° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04902338 |
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| Source dataset | uspto-grants-1990_02 |
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| ORD ID | ord-090fe35299ce4bec84cc2eab37e08e2e |
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| Source note | uspto-grants-1990_02 |
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