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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855223Generated: October 30, 2026

3-Bromo-1,1,1-Trifluoro-2-Propanol → HCID 87793684, compound

https://huagongshe.com/reaction/855223

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-1,1,1-Trifluoro-2-PropanolHCID 220632—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 59344854HCID 59344854—
SolventAcetonitrileHCID 6342—
ProductHCID 87793684HCID 8779368430%

Reaction Steps

260 mg of N-(4-tert-butyl-benzyl)-2,2,2-trifluoro-acetamide (1 mmol) were dissolved in 10 ml acetonitrile and treated with 169 mg of potassium tert-butylate (1.5 mmol). After 5 min stirring at rt, 0.125 ml of [rac]-3-bromo-1,1,1-trifluoro-propan-2-ol (1.2 mmol) were added and the reaction mixture stirred at 75° C. bath temperature for 22 h. After cooling down to rt, the reaction mixture was concentrated in vacuo, dissolved in EtOAc/water and the phases separated. The organic phase was then washed with brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography (90 g silica gel; EtOAc/heptane 1:4) to give 111 mg of N-(4-tert-butyl-benzyl)-2,2,2-trifluoro-N-(3,3,3-trifluoro-2-hydroxy-propyl)-acetamide as a white solid (30%). MS (ISP) 301.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-2c2ba4a7d5e5439a813a868e8b1fd947
Source noteuspto-grants-2007_08