HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57339Generated: October 29, 2026
4,4,4-Trifluorovaline → 2-Amino-4,4,4-trifluoro-3-methylbutan-1-ol
https://huagongshe.com/reaction/57339
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4,4,4-Trifluorovaline | HCID 259831 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Amino-4,4,4-trifluoro-3-methylbutan-1-ol | HCID 9877444 | — |
Reaction Steps
To a chilled (00° C.) solution of 2-amino-4,4,4-trifluoro-3-methylbutanoic acid (736 mg, 4.30 mmol) in THF (9 mL) was added aluminum (111) lithium hydride (2.26 mL, 9.03 mmol, 4M) dropwise. After addition complete, the reaction was allowed to stir at ambient temperature for 1 hour. Cool to 0° C. and quench w/sat. Na2SO4 soln, added EtOAc (50 mL), Na2SO4, filtered, conc. in vacuo afforded material that was a mixture of the title compound and the starting material acid in a 3:2 ratio which was used crude in the next step. 1H NMR (400 MHz, CDCl3) δ 3.71 (dd, J=10.7, 3.7 Hz, 1H), 3.57 (dd, J=10.4, 5.2 Hz, 1H), 3.45 (ddd, J=10.7, 8.0, 4.8 Hz, 2H), 3.28 (ddd, J=8.2, 5.3, 2.9 Hz, 1H), 3.06 (td, J=7.3, 3.6 Hz, 1H), 2.44-2.20 (m, 2H), 2.04-1.54 (m, 1H), 1.21-1.08 (m, 7H). 19F NMR (376 MHz, CDCl3) δ−68.33 (s), −70.12 (s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434719B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-0308faff7ca4409aabf50c68522aeb07 |
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| Source note | uspto-grants-2016_09 |
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