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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4,4-TrifluorovalineHCID 259831—
ReactantAluminumHCID 5359268—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-4,4,4-trifluoro-3-methylbutan-1-olHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434719B2
Source datasetuspto-grants-2016_09
ORD IDord-0308faff7ca4409aabf50c68522aeb07
Source noteuspto-grants-2016_09