HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500052Generated: October 29, 2026
L-Methionine → methyl (2S)-2-amino-4-(methylsulfanyl)butanoate
https://huagongshe.com/reaction/500052
Participants
| Role | Name | HCID | Charge |
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| Reactant | L-Methionine | HCID 6137 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | methyl (2S)-2-amino-4-(methylsulfanyl)butanoate | HCID 64684 | — |
Reaction Steps
At about 0° C., acetyl chloride (15 mL) was added dropwise to methanol (100 mL). After stirring for about 10 minutes at about 0° C., L-methionine (8.5 g, 57 mmol) was added and the resulting solution was stirred for about 10 minutes. The solution was then heated at reflux for about 4 hours, and then maintained at ambient temperature for about 16 hours. The solvent was removed in vacuo, the resulting residue was dissolved in chloroform (100 mL), and the solution was neutralized to pH 7-8 by the careful addition of a saturated aqueous sodium bicarbonate solution. Following standard extractive workup with chloroform, the resulting residue was kept under high vacuum for about two hours to afford the title product as a colourless oily liquid, which was used directly in the next step without any further purification (crude yield 6 g, 65%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767860B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-4e939417f46d44a78ab7ccf1782ddaee |
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| Source note | uspto-grants-2010_08 |
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