HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807938Generated: October 31, 2026
Trifluoroacetic acid → (S)-2-amino-4-(5-trifluoromethyl-pyridin-2-yloxy)-butan-1-ol
https://huagongshe.com/reaction/1807938
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (S)-2,2-dimethyl-4-[2-(5-trifluoromethyl-pyridin-2-yloxy)-ethyl]-oxazolidine-3-carboxylic acid tert-butyl ester | HCID 59173205 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (S)-2-amino-4-(5-trifluoromethyl-pyridin-2-yloxy)-butan-1-ol | HCID 59173196 | 113.6% |
Reaction Steps
To a solution of trifluoroacetic acid (0.23 ml) in water (9 ml) was added dropwise a solution of (S)-2,2-dimethyl-4-[2-(5-trifluoromethyl-pyridin-2-yloxy)-ethyl]-oxazolidine-3-carboxylic acid tert-butyl ester (390 mg) in acetonitrile (1.5 ml). The mixture was heated for 90 min at 80° C. with stirring. The mixture was then cooled to room temperature and made basic by addition of 2 M aq. sodium hydroxide solution, then diluted with ethyl acetate and washed sequentially with water and with saturated brine. The organic phase was separated, dried over sodium sulphate and concentrated in vacuo to give (S)-2-amino-4-(5-trifluoromethyl-pyridin-2-yloxy)-butan-1-ol (284 mg, quant.) as a yellow oil. MS (ISP): 251.2 ([M+H]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357712B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-e8cc73cfb5fb44beb5b36558cb9865a1 |
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| Source note | uspto-grants-2013_01 |
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