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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510634Generated: November 1, 2026

Chlorotrimethylsilane → 2-(4-Bromo-2-chlorophenyl)ethanamine

https://huagongshe.com/reaction/510634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantLithium borohydrideHCID 4148881—
Reactant4-Bromo-2-chloro-1-(2-nitroethenyl)benzeneHCID 67080459—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Bromo-2-chlorophenyl)ethanamineHCID 6708032895%

Reaction Steps

To a stirred suspension of lithium borohydride (0.29 g, 13 mmol) in tetrahydrofuran (20 mL) at ambient temperature was added chlorotrimethylsilane (3.4 mL, 27 mmol), dropwise over 2 minutes. After stirring at ambient temperature for 20 minutes, argon gas was bubbled through the mixture for 2 minutes to remove the remaining trimethylsilane that had formed. A solution of 4-bromo-2-chloro-1-(2-nitrovinyl)benzene (0.88 g, 3.4 mmol) in tetrahydrofuran (15 mL) was added dropwise over 4 minutes with stirring at ambient temperature. The resulting mixture was stirred and heated to reflux for 1 hour. The mixture was cooled in an ice bath and carefully quenched with methanol (20 mL). The solvent was evaporated, and the residue was partitioned between 20% potassium hydroxide (40 mL) and dichloromethane (20 mL). The organic layer was dried over sodium sulfate and concentrated to afford 2-(4-bromo-2-chlorophenyl)ethanamine as a light yellow oil (0.75 g, 95% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096567B2
Source datasetuspto-grants-2015_08
ORD IDord-2933305063db4015946a9677059c51ea
Source noteuspto-grants-2015_08