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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromo-1,1,1-Trifluoro-2-Propanol | HCID 220632 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 59344854 | HCID 59344854 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 87793684 | HCID 87793684 | 30% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07259183B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-2c2ba4a7d5e5439a813a868e8b1fd947 |
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| Source note | uspto-grants-2007_08 |
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