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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888631Generated: November 3, 2026

2,2,2-Trifluoroethanol → HCID 178441287, compound

https://huagongshe.com/reaction/1888631

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178441283HCID 178441283—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductTrifluoroacetic acidHCID 64220.1%
ProductHCID 178441287HCID 17844128756.1%

Reaction Steps

A mixture of the product from Example 47A (101 mg, 0.27 mmol), trifluoroethanol (33 mg, 0.32 mmol) and potassium tert-butoxide (2 M) (340 μL, 0.68 mmol) in THF (10 mL) was stirred at rt for 12 hrs. The mixture was diluted with water, and extracted with EtOAc. The organic extract was dried (Na2SO4), filtered and concentrated. The residue was purified by reverse phase preparative HPLC on a Waters Symmetry C8 column (25 mm×100 mm, 7 μm particle size) using a gradient of 10% to 100% acetonitrile:0.1% aqueous trifluoroacetic acid over 8 minutes (10 minutes run time) at a flow rate of 40 mL/minute to afford 34 mg (28%) of the title compound. 1H NMR (400 MHz, CDCl3) δ ppm 0.97 (t, J=7.36 Hz, 3 H) 1.37-1.48 (m, 2 H) 1.65-1.75 (m, 2 H) 1.68 (s, 9 H) 4.50 (q, J=8.59 Hz, 2 H) 7.05 (d, J=8.59 Hz, 1 H) 7.34 (dd, J=8.90, 2.76 Hz, 1 H) 7.97 (s, 1 H) 8.11 (d, J=2.76 Hz, 1 H); MS (DCI/NH4+) m/z 449 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501794B2
Source datasetuspto-grants-2013_08
ORD IDord-6788442e50f74970a89790f336ea1095
Source noteuspto-grants-2013_08