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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021348Generated: October 31, 2026

Chlorotrimethylsilane → 2-(2,4-Dichloro-6-methoxyphenyl)ethanamine

https://huagongshe.com/reaction/1021348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantLithium borohydrideHCID 4148881—
Reactant1,5-Dichloro-3-methoxy-2-(2-nitrovinyl)benzeneHCID 67080898—
SolventTetrahydrofuranHCID 8028—
Product2-(2,4-Dichloro-6-methoxyphenyl)ethanamineHCID 6708030996.8%

Reaction Steps

To a stirred suspension of lithium borohydride (0.20 g; 9.0 mmol) in 15 mL tetrahydrofuran at ambient temperature was added chlorotrimethylsilane, dropwise over 2 minutes. Gas was evolved and the mixture warmed slightly. After stirring for 20 minutes, gas evolution had ceased, and argon gas was bubbled through the mixture for 2 minutes to remove the remaining trimethylsilane that had formed. A solution of 1,5-dichloro-3-methoxy-2-(2-nitrovinyl)benzene (0.56 g; 2.3 mmol) in 10 mL THF was then added dropwise with stirring at ambient temperature over 4 minutes. The resulting mixture was then stirred and heated to reflux. After 90 minutes, the heat was removed, and after cooling to ambient temperature, the mixture was cooled in an ice bath and carefully quenched with 15 mL of methanol. The solvent was evaporated, and the residue was partitioned between 30 mL of 20% KOH and 15 mL of dichloromethane. The organic layer was dried over sodium sulfate and evaporated to give 0.49 g of 2-(2,4-dichloro-6-methoxyphenyl)ethanamine as a cloudy yellow oil. MS (apci, pos) m/z=220.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716498B2
Source datasetuspto-grants-2014_05
ORD IDord-29b9d4d5de7c4d2986b70718f83aab9a
Source noteuspto-grants-2014_05