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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659203Generated: October 26, 2026

N,N,N',N'-Tetramethylethylenediamine → 2-Bromo-6-methoxy-4-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/659203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant1,2-Dibromo-1,1,2,2-tetrachloroethaneHCID 69426—
Reactant2-Methoxy-4-(trifluoromethyl)benzoic acidHCID 3690873—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexaneHCID 8078—
Product2-Bromo-6-methoxy-4-(trifluoromethyl)benzoic acidHCID 5943842312%

Reaction Conditions

Temperature-75 °C

Reaction Steps

To −75° C. cooled THF (70 ml) was added dropwise 36 ml (50.0 mmol) of a 1.4 M sec-BuLi solution in cyclohexane within 5 minutes keeping the temperature below −70° C. 7.5 ml (50.0 mmol) TMEDA were added dropwise at temperature below −70° C. within 5 minutes. A solution of 5.0 g (22.71 mmol) 2-methoxy-4-(trifluoromethyl)benzoic acid (commercial) in THF (25 ml) was added dropwise at over a period of 20 minutes. The dark green solution was stirred at −75° C. for 2 hours. A solution of 29.6 g (90.84 mmol) 1,2-dibromotetrachloroethane in THF (30 ml) was added dropwise. The off-white suspension was stirred at −75° C. for 1 hour and then allowed to warm to room temperature. The yellow solution was quenched by dropwise addition of 60 ml water under ice bath cooling. The mixture was diluted with ethyl acetate (70 ml) and water (30 ml). The aqueous layer was extracted with ethyl acetate (50 ml), acidified with HCl 25% and extracted with ethyl acetate (3×50 ml). The extracts were combined, dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was stirred in heptane, filtered and dried. The solid was recrystallized from heptane (7 ml) and ethyl acetate (2 ml) to provide 815 mg (12%) of the title compound as a white solid. MS (m/e): 298.9 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08080541B2
Source datasetuspto-grants-2011_12
ORD IDord-b76ff44ac251496d8d6332b323985024
Source noteuspto-grants-2011_12