Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (+-)-Methionine | HCID 876 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178488674 | HCID 178488674 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178515872 | HCID 178515872 | 104.4% |
Reaction Steps
To a round-bottomed flask was added D,L-methionine (1.19 g, 7.96 mmol), 3-(4-methoxyphenyl)-pyrazole (990 mg, 5.68 mmol), and methanesulfonic acid (23 ml). The resulting solution was heated to about 50° C. for about forty-eight hours, and was then allowed to cool to room temperature and poured into water. The pH of the solution was adjusted to about 7 with 5 N sodium hydroxide, and was then extracted with ethyl acetate. The organic extracts were dried over magnesium sulfate, filtered, and concentrated in vacuo to afford 950 mg of a white solid which was determined to be about 95% pure by NMR. This material was subsequently employed directly without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06689888B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-c350c59d444f40a9ae5cfd31ef20114d |
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| Source note | uspto-grants-2004_02 |
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