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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620647Generated: November 2, 2026

Trifluoroacetic acid → (R)-2-aminobut-3-yn-1-ol trifluoroacetate

https://huagongshe.com/reaction/1620647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl (4R)-4-ethynyl-2,2-dimethyl-1,3-oxazolidine-3-carboxylateHCID 11096274—
SolventMethanolHCID 887—
Product(R)-2-aminobut-3-yn-1-ol trifluoroacetateHCID 86678813—

Reaction Steps

To a solution of (R)-tert-butyl 4-ethynyl-2,2-dimethyloxazolidine-3-carboxylate (680 mg) (Tetrahedron 1996, 52, 11215.) in methanol (20 mL) was added trifluoroacetic acid (0.23 mL). The reaction mixture was stirred at room temperature for 4 hr and concentrated under reduced pressure to give the title compound (623 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-5e0e3acfe6a741fa83d51040380aea2c
Source noteuspto-grants-2014_07