HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464656Generated: October 29, 2026
Sodium Hydroxide → 5-(2-hydroxyethyl)-6-methyl-2-[(1-methyl-2-oxopropyl)thio]-4(3H)-pyrimidinone
https://huagongshe.com/reaction/464656
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Chloro-2-butanone | HCID 20026 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N,N,N-triethylbenzeneethanaminium chloride | HCID 20262408 | — |
| Reactant | HCID 178433550 | HCID 178433550 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(2-hydroxyethyl)-6-methyl-2-[(1-methyl-2-oxopropyl)thio]-4(3H)-pyrimidinone | HCID 135674650 | — |
Reaction Steps
A mixture of 30 parts of 4-hydroxy-2-mercapto-6-methyl-5-pyrimidineethanol, 6.8 parts of sodium hydroxide, 15 parts of sodium hydrogen carbonate and 100 parts of 2-propanone was stirred at room temperature and there were added 180 parts of tetrahydrofuran and 170 parts of water. Then there were added at once 25 parts of 3-chloro-2-butanone and 0.2 parts of N,N,N-triethylbenzeneethanaminium chloride and the whole was stirred and heated for 1 hour at 60° C. Stirring was continued overnight at room temperature. The reaction mixture was filtered and the filtrate was salted out. The organic phase was separated, dried, filtered and evaporated, yielding 36 parts of 5-(2-hydroxyethyl)-6-methyl-2-[(1-methyl-2-oxopropyl)thio]-4(3H)pyrimidinone as an oily residue (intermediate 7).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04548938 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-4f89a95843844bf28928341210f69966 |
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| Source note | uspto-grants-1985_10 |
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