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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266922Generated: October 30, 2026

Chlorotrimethylsilane → 2-Amino-4,4,4-trifluorobutan-1-ol

https://huagongshe.com/reaction/2266922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
Reactant2-Amino-4,4,4-trifluorobutanoic acidHCID 353083—
ReactantLithium borohydrideHCID 4148881—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-4,4,4-trifluorobutan-1-olHCID 5341643338%

Reaction Steps

A solution of trimethylsilyl chloride (1.38 g, 12.73 mmol) was added to a solution of lithium borohydride (3.2 mL, 2.0 M in THF) and THF (5 mL) at 25° C. After stirring 5 min, 2-amino-4,4,4-trifluoro-butyric acid (0.50 g, 3. 18 mmol) was added portionwise over a 5 min period. The reaction was allowed to stir 48 h. The reaction was quenched by cautious addition of MeOH (5 mL) dropwise. The solvent was evaporated and the residue treated with potassium hydroxide (KOH) solution (20%, 6 mL). The aqueous phase was extracted using dichloromethane, 3 times (10 mL each). The organic phases were combined and dried over anhydrous sodium sulfate. After filtration the solvent was evaporated to afford the 2-amino-4,4,4-trifluoro-butan-1-ol as an oil (0.174 g, 38%). This oil was used directly in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858658B2
Source datasetuspto-grants-2010_12
ORD IDord-0c573a34d5684858b6b1c19706525412
Source noteuspto-grants-2010_12