Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-Bromo-5-(trifluoromethyl)benzaldehydeHCID 16115438—
SolventDichloromethaneHCID 6344—
Product1-[3-bromo-5-(trifluoromethyl)phenyl]-N,N-dimethylmethanamineHCID 5943940374%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513421B2
Source datasetuspto-grants-2013_08
ORD IDord-fab43daa7c1f4aba9155650bb40bd533
Source noteuspto-grants-2013_08