Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Phenyl Isothiocyanate | HCID 7673 | — |
| Reactant | HCID 178508113 | HCID 178508113 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 178518524 | HCID 178518524 | — |
Reaction Steps
75 g of 5-amino-2,4,6-trihydroxypyrimidine was dissolved in 1.5 to 5% sodium hydroxide with vigorous overhead stirring producing a violet solution. The reaction was heated to 60° C. and 63 ml phenyl isothiocyanate was added dropwise over 1.5 hours. The reaction turned pale yellow. The reaction was stirred an additional 2 hours at 60° C., cooled and acidified with glacial acetic acid producing a light yellow precipitate. This was filtered to yield about 75 g of N-(2,4,6-trihydroxy-5-pyrimidyl)-N'-phenylthiourea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05064947 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-da6ce894c9d14acc80b9c38aa81d30ed |
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| Source note | uspto-grants-1991_11 |
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