HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23224Generated: October 30, 2026
Water → (1S)-2-(3,5-difluorophenyl)-1-[(2S)-oxiran-2-yl]ethylamine
https://huagongshe.com/reaction/23224
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | (2S,3S)-3-amino-1-chloro-4-(3,5-difluorophenyl)butan-2-ol | HCID 9834600 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (1S)-2-(3,5-difluorophenyl)-1-[(2S)-oxiran-2-yl]ethylamine | HCID 86587041 | — |
Reaction Steps
(1S,2S)-3-chloro-1-(3,5-difluorobenzyl)-2-hydroxypropylamine (EXAMPLE 17, 33 mg, 0.14 mmol) and absolute ethanol (1.5 mL) are mixed. Potassium hydroxide (9.8 mg, 0.175 mmol) in absolute ethanol (0.5 mL) is added to this mixture and the resulting mixture is stirred at 20-25 deg for 30 min. At this time ESMS indicates formation of the product (MH+=200.1). Water (2 mL) is added and mixture is concentrated under reduced pressure to half the volume and then diluted with ethyl acetate (15 mL). The organic phase is separated and the aqueous phase is extracted with ethyl acetate (2×10 mL). The organic phases are combined, washed with saline and dried over anhydrous magnesium sulfate. The solvent is removed under reduced pressure to give the title compound, MH+=200.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06849750B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-8e6d2cc776094ec2bc85a80df389e8fb |
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| Source note | uspto-grants-2005_02 |
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