HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051750Generated: November 1, 2026
Methanesulfonyl chloride → HCID 118103467, compound
https://huagongshe.com/reaction/1051750
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Amino-4-(2,4,5-trifluorophenyl)butanoic acid | HCID 23146023 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 118103467 | HCID 118103467 | 96.9% |
Reaction Steps
To the rapidly stirred 80° C. suspension of methanesulfonyl chloride (0.88 g, 7.72 mmol) and sodium bicarbonate (3.24 g, 38.6 mmol) in acetonitrile (400 mL), 3-amino-4-(2,4,5-trifluorophenyl)butanoic acid ((±)-Ia, 1.5 g, 6.43 mmol) is added over period of 2 h. The resulting suspension was further stirred for 16 h at 80° C., after which time the fine suspension was cooled to 0° C. and filtered. The filtrate was evaporated under reduced pressure to afford 1.34 g (96% yield) of racemic 4-(2,4,5-trifluorobenzyl)azetidin-2-one ((±)-IIa) as pale yellow crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09388188B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-4ed0499a4ea74ce0a773a8c3de95cb9f |
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| Source note | uspto-grants-2016_07 |
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