Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985978Generated: November 2, 2026

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

https://huagongshe.com/reaction/1985978

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 5341643338.2%

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 numberUS07547725B2
Source datasetuspto-grants-2009_06
ORD IDord-f05b3188e6c5405da193846d7b2effe3
Source noteuspto-grants-2009_06