Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4,6-Dimethyl-2-methylsulfonylpyrimidine | HCID 2772382 | — |
| Reactant | Methyl 2-hydroxy-3,3-dimethylbutanoate | HCID 9855510 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 15070275 | HCID 15070275 | 83.9% |
Reaction Steps
2.9 g of methyl 2-hydroxy-3,3-dimethybutyrate, 4.1 g of 4,6 -dimethyl-2-methylsulfonylpyrimidine and 3.3 g of potassium carbonate were added to 50 ml of N,N-dimethylformamide, and the mixture was stirred at 100° C. for 4 hours. The reaction solution was cooled to room temperature, poured into water and extracted with 100 ml of ethyl acetate. The organic layer was washed twice with a sodium chloride aqueous solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The liquid substance thereby obtained was purified by silica gel column chromatography (eluent: hexane/ethyl acetate =6/1) to obtain 4.2 g of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04968340 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-93c1f599379a44d6846451f41d515ed7 |
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| Source note | uspto-grants-1990_11 |
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