HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894961Generated: November 2, 2026
Dimethylamine → 1-[3-bromo-5-(trifluoromethyl)phenyl]-N,N-dimethylmethanamine
https://huagongshe.com/reaction/1894961
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 3-Bromo-5-(trifluoromethyl)benzaldehyde | HCID 16115438 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[3-bromo-5-(trifluoromethyl)phenyl]-N,N-dimethylmethanamine | HCID 59439403 | 74% |
Reaction Steps
To a solution of 3-bromo-5-(trifluoromethyl)benzaldehyde (30 g, 118.6 mmol) in methylene chloride (150 mL) was added dimethylamine (2.0 M in THF, 118 mL) and the reaction was stirred at room temperature for 15 min. The reaction was cooled to 0° C. and sodium triacetoxyborohydride (37.7 g, 178 mmol) was added. The resulting mixture was warmed to room temperature and stirred for 3 h. The solvents were removed under reduced pressure and saturated sodium bicarbonate solution was added. The resulting mixture was extracted three times with ethyl acetate. The combined extracts were washed with brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. Silica gel chromatography (90/10 to 60/40 ethyl acetate/hexanes gradient) provided 1-[3-bromo-5-(trifluoromethyl)phenyl]-N,N-dimethylmethanamine as a colorless oil (Int-8, 24.9 g, 74% yield). LC-MS: (FA) ES+ 282; 1H NMR (300 MHz, CDCl3) δ ppm 7.68 (s, 1H), 7.65 (s, 1H), 7.52 (s, 1H), 3.44 (s, 2H), 2.25 (s, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513421B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-fab43daa7c1f4aba9155650bb40bd533 |
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| Source note | uspto-grants-2013_08 |
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