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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624101Generated: November 1, 2026

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

https://huagongshe.com/reaction/1624101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant2-Amino-4,4,4-trifluorobutanoic acid hydrochlorideHCID 2756566—
ReactantLithium borohydrideHCID 4148881—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-4,4,4-trifluorobutan-1-olHCID 53416433—

Reaction Steps

0.32 ml (0.65 mmol) of lithium borohydride (2 M in THF) were initially charged in 0.5 ml of dry THF, 0.16 ml (1.28 mmol) of chlorotrimethylsilane were added at RT and the mixture was stirred at RT for 5 min. 50 mg (0.26 mmol) of 2-amino-4,4,4-trifluorobutanoic acid hydrochloride (1:1) were then added a little at a time, and the reaction mixture was stirred at RT overnight. 0.5 ml of methanol was added, and the mixture was then concentrated. 0.6 ml of a 20% strength solution of potassium hydroxide was then added to the residue, and the mixture was extracted three times with dichloromethane. The combined organic phases were dried over sodium sulphate, filtered and concentrated. This gave 33 mg of the target compound (88% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778964B2
Source datasetuspto-grants-2014_07
ORD IDord-99d8d13ecf9c4f85839342cd4100d489
Source noteuspto-grants-2014_07