HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247850Generated: November 2, 2026
Potassium Hydroxide → HCID 136464294, compound
https://huagongshe.com/reaction/2247850
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methylthiouracil | HCID 667493 | — |
| Reactant | HCID 67946610 | HCID 67946610 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 136464294 | HCID 136464294 | 47% |
Reaction Steps
0.71 g (5 mmol) of 6-methyl-2-thiouracil and 0.65 g (11.7 mmol) of potassium hydroxide are dissolved in 10 ml of water. Simultaneously, 1.22 g (5.5 mmol) of 2-chloromethyl-5-ethyl-4-methoxypyridinium chloride (m.p.: 123°-125° C.) and 0.1 g of tetrabutylammonium chloride are dissolved in 10 ml of chloroform. After combining the two solutions the reaction mixture is vigorously stirred at room temperature for 20 hours. After separating the phases the aqueous layer is extracted 3 times with 5 ml of chloroform each, the combined organic phase is washed with sodium chloride solution, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The residue is thoroughly triturated with ethyl acetate, filtered and the crude product obtained is recrystallized from ethanol to obtain 0.68 g (47%) of the title compound in the form of white crystals, m.p.: 167°-168° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05037830 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-517fc6150db64ae79af94e1b3c22acf6 |
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| Source note | uspto-grants-1991_08 |
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