Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 6-Chloro-1,3-dimethyl-2,4(1H,3H)-pyrimidinedione | HCID 81442 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12742739 | HCID 12742739 | 71.9% |
Reaction Steps
To 70 ml of an acetonitrile solution containing 21 g of 6-chloro-1,3-dimethyluracil thus-obtained was added 16 g of N-chlorosuccinimide under cooling with ice (at the solution temperature of 5° C). The temperature was gradually raised to 35° C. After further stirring for 1 hour, 70 ml of water was added to the reaction solution, and the crystals thus-deposited were collected by filtration, washed with a cold solvent mixture of 18 ml of acetonitrile and 18 ml of water and dried to obtain 18 g of 5,6-dichloro-1,3-dimethyluracil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05066573 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-70d6d93462954f0a80b8d86106e4109c |
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| Source note | uspto-grants-1991_11 |
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