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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405566Generated: November 3, 2026

HCID 65327287, compound → HCID 65322753, compound

https://huagongshe.com/reaction/1405566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 65327287HCID 65327287—
SolventTetrahydrofuranHCID 8028—
ProductHCID 65322753HCID 65322753—

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a 250-mL round-bottom flask, was placed a solution of 3-(2-bromo-5-methoxyphenyl)propanenitrile (2.39 g, 10.00 mmol, 1.00 equiv) in tetrahydrofuran (40 mL). This was followed by the addition of BH3 solution in tetrahydrofuran (30 mL, 3.00 equiv) dropwise with stirring at 0° C. The resulting solution was stirred for 6 hs at 20° C. in an oil bath. The reaction was then quenched by the addition of water. The resulting solution was concentrated under vacuum. The residue was diluted in water. The pH value of the aqueous solution was adjusted to 8-9 with 1N sodium hydroxide. The resulting aqueous solution was extracted with 10×50 mL of dichloromethane. The organic layers was combined and dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 2.23 g (crude) of 3-(2-bromo-5-methoxyphenyl)propan-1-amine as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916560B2
Source datasetuspto-grants-2014_12
ORD IDord-b26007cfd9ec495fa9b110e156329ca5
Source noteuspto-grants-2014_12