Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloral | HCID 6407 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 21497484 | HCID 21497484 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 68144560 | HCID 68144560 | — |
Reaction Steps
1-allyl-3-methyl-5-iminoimidazolidine-2,4-dione (20.0 g -- 0.12 mol) and 17.7 g (0.12 mol) chloral in 50 ml chloroform were stirred at 25° C. for 1/2 hour. To the resulting solution was added 28.69 (0.24 mol) thionyl chloride. The temperature rose to 35° C. and a precipitate formed. The reaction mixture was heated at 55° C. for 2 hours, cooled and filtered. The filtrate was stripped to give 24 g of 1-allyl-3-methyl-5-(1,2,2,2-tetrachloroethylimino)-imidazolidine-2,4-dione, as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03992402 |
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| Source dataset | uspto-grants-1976_11 |
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| ORD ID | ord-f4a1c949d9784ec5af181a1e2fcfcac9 |
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| Source note | uspto-grants-1976_11 |
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