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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855191Generated: October 27, 2026

4-tert-Butylbenzaldehyde → (4-Tert-butylbenzyl)-[2-(3,4-dichloro-phenyl)-ethyl]-amine

https://huagongshe.com/reaction/855191

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylbenzaldehydeHCID 70324—
Reactant3,4-DichlorophenethylamineHCID 217958—
ReactantSodium borohydrideHCID 4311764—
CatalystHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
Product(4-Tert-butylbenzyl)-[2-(3,4-dichloro-phenyl)-ethyl]-amineHCID 68563688102.1%

Reaction Steps

0.38 ml of 4-tert-butylbenzaldehyde (2.25 mmol) and 0.227 ml 2-(3,4-dichloro-phenyl)-ethylamine (1.5 mmol) were dissolved in 4.5 ml methanol at rt, and after stirring for 30 min at rt, were refluxed for 2 h. After cooling down to rt, 85 mg (2.25 mmol) sodium borohydride were added and after stirring for 5 min at rt, the reaction mixture was then refluxed for 2 h. After cooling down to rt, the reaction mixture was treated with 4 drops 1 N HCl and concentrated in vacuo. The residue was diluted with water/EtOAc. After separation of the organic phase, the aqueous phase was extracted with EtOAc and the combined organic phases were washed with brine, dried with magnesium sulfate, filtered off and concentrated in vacuo. The residue was purified by column chromatography (40 g silica gel; EtOAc/heptane 1:2) to give 515 mg colorless viscous oil (97%). MS (ISP) 336.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-a02975908a8e478080f745e3b6bffaa2
Source noteuspto-grants-2007_08