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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708058Generated: November 3, 2026

Hydrochloric Acid → (4-Bromo-3-methylphenyl)methanamine

https://huagongshe.com/reaction/1708058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBoraneHCID 6331—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Bromo-3-methylbenzonitrileHCID 2737494—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductAmmoniaHCID 222—
Product(4-Bromo-3-methylphenyl)methanamineHCID 2175614371.3%

Reaction Steps

Borane in THF (25.5 ml) was added dropwise, at 0° C., under nitrogen to a solution of 4-bromo-3-methylbenzonitrile (1.0 g) in THF (dry, 20 ml). The solution was left at 0° C. for 30 min and then stirred at room temperature overnight. Methanol was added carefully to quench the reaction. Hydrochloric acid (2N, 20 ml) was added and the solution stirred at room temperature for 4 h. Further 2N hydrochloric acid (20 ml) was added and the mixture heated to reflux for several hours. Sodium bicarbonate was added to the cooled mixture till basic and extracted with dichloromethane (4×50 ml), dried and slowly evaporated to give an orange/yellow oil. This was then applied in methanol to a flash column of silica gel which was eluted with hexane: ethyl acetate (1:1)→ethyl acetate:methanol:0.88 ammonia (790:200:10) to give the title compound as a yellow/orange oil (364 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05356893
Source datasetuspto-grants-1994_10
ORD IDord-f05e3cdc0a994c838c1b3a558abc467d
Source noteuspto-grants-1994_10