Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 20537580 | HCID 20537580 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20537582 | HCID 20537582 | — |
Reaction Steps
After dilution with 200 ml of tetrahydrofurane, 34 g of 3-amino-1-(3,5-dichlorophenyl)pyrrolidine-2,5-dione hydrobromide (obtained in Example 2b) are added at -20° C. to 104 ml of a 20% solution of phosgene in toluene. Then 27.9 g of triethylamine in 100 ml of tetrahydrofurane are added dropwise at -37° to -28° C. and the reaction mixture is thereafter stirred for a further 12 hours at -33° C. to bring the reaction to completion. The precipitate is collected by filtration at -20° C. and the solution is concentrated. The 3-(N-chlorocarbonylamino)-1-(3,5-dichlorophenyl)pyrrolidine-2,5-dione obtained is used direct for the consequent reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04332816 |
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| Source dataset | uspto-grants-1982_06 |
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| ORD ID | ord-0a337038eb594658996fe7aabaa1c099 |
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| Source note | uspto-grants-1982_06 |
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