Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277583Generated: October 26, 2026

Diethyl Ether → m-Chloroamphetamine

https://huagongshe.com/reaction/2277583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantAcetonitrileHCID 6342—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 178478996HCID 178478996—
SolventTetrahydrofuranHCID 8028—
Productm-ChloroamphetamineHCID 2002747011.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 3-chlorobenzylmagnesium chloride (0.1 mol) in anhydrous ether (100 mL) (prepared from 3-chlorobenzyl chloride (16.1 g, 0.1 mol) and magnesium turnings (2.4 g, 0.1 mol) in anhydrous ether (100 mL)) was added anhydrous acetonitrile (4.1 g, 0.1 mol) dropwise at room temperature. When the reaction mixture was stirred at 60° C. for 3 hours, it was cooled to 0° C. followed by addition of THF (50 mL). Lithium aluminum hydride (4.2 g, 0.1 mol) was then added cautiously into the above reaction mixture and it was heated to reflux temperature for 3 hours. Ice-water was added to quench the reaction. After partitioning between ether and H2O, the separated organic layer was washed with brine, dried over anhy. Na2SO4, filtered and concentrated in vacuo. Flash column chromatography separation (silica gel, 180 g, 5% methanol in DCM) then yielded the title compound as yellowish oil (1.9 g, 11%). MS: 170.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133158B2
Source datasetuspto-grants-2015_09
ORD IDord-66c53230c8d3475cb1997a70938f618d
Source noteuspto-grants-2015_09