Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855220Generated: October 28, 2026

Hydrochloric Acid → (4-Tert-butyl-benzyl)-[2-(3-difluoromethoxy-phenyl)-ethyl]-amine

https://huagongshe.com/reaction/855220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant4-tert-ButylbenzaldehydeHCID 70324—
ReactantSodium borohydrideHCID 4311764—
Reactant2-[3-(Trifluoromethoxy)phenyl]ethan-1-amine hydrochlorideHCID 57438503—
SolventMethanolHCID 887—
Product(4-Tert-butyl-benzyl)-[2-(3-difluoromethoxy-phenyl)-ethyl]-amineHCID 6857681989%

Reaction Steps

0.55 ml of 4-tert-butylbenzaldehyde (9.19 mmol), 1.37 g of 2-(3-trifluoromethoxy-phenyl)-ethylamine hydrochloride (6.13 mmol) and 0.304 g of potassium carbonate (6.13 mmol) were suspended in 18 ml methanol at rt, and after stirring for 30 min at rt, were refluxed for 2.5 h. After cooling down to rt, 348 mg (9.19 mmol) of sodium borohydride were added and after stirring for 5 min at rt, the reaction mixture was refluxed for 22 h. After cooling down to rt, the reaction mixture was treated with 0.4 ml 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 to give 1.82 g off-white oil (89%). MS (ISP) 334.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-ef7b0242438a4f9f91a856fe98ebf1ee
Source noteuspto-grants-2007_08