HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876378Generated: October 30, 2026
Hydrochloric Acid → HCID 71093016, compound
https://huagongshe.com/reaction/876378
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 86712809 | HCID 86712809 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 71093016 | HCID 71093016 | 78% |
Reaction Steps
A solution of 2-methyl-propane-2-sulfinic acid [(S)-2,2-difluoro-1-fluoromethyl-1-(2-fluoro-phenyl)-3-hydroxy-propyl]-amide (intermediate F4.1) (145.5 mg, 426 μmol) in methanol (2.5 ml) was cooled to 0° C. and treated with hydrochloric acid (4 M in dioxane; (533 μl, 2.13 mmol). The solution was left to warm to room temperature and stirred for 1 hour. After removal of the solvent at reduced pressure the solid residue was dissolved in water (5 ml), then extracted with ethyl acetate (2×10 ml). The organic layers were extracted with water (5 ml), thereafter the combined aqueous layers treated with a solution of sodium carbonate (2 M) to adjust the pH to 9-10. Extraction with ethyl acetate (3×35 ml), combination of the organic layers and evaporation at reduced pressure after drying over sodium sulphate yielded the crude (S)-3-amino-2,2,4-trifluoro-3-(2-fluoro-phenyl)-butan-1-ol (78 mg, 78% yield) as a colorless oil. Evaporation of the first 2 ethyl acetate layers followed by the treatment with a solution of sodium carbonate and proceeding as described above yielded another fraction (22 mg) of product. MS (ISN): m/z=238.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987255B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-29507457c0c54b0e8326552ab3da4388 |
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| Source note | uspto-grants-2015_03 |
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