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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474569Generated: October 25, 2026

Sodium borohydride → 2-(4-(4-Chloro-3-(trifluoromethyl)phenoxy)phenyl)ethanamine

https://huagongshe.com/reaction/474569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantChloro-4-(4-(2-nitroethyl)phenoxy)-2-(trifluoromethyl)benzeneHCID 67775633—
CatalystDichloronickel;hexahydrateHCID 11791229—
SolventMethanolHCID 887—
Product2-(4-(4-Chloro-3-(trifluoromethyl)phenoxy)phenyl)ethanamineHCID 6777554857%

Reaction Steps

To the mixture of 1-chloro-4-(4-(2-nitroethyl)phenoxy)-2-(trifluoromethyl)benzene (17 g, 49.2 mmol) and nickel(II) chloride hexahydrate (46.6 g, 197 mmol) in methanol (300 mL) at 0° C. was added NaBH4 (3.72 g, 98 mmol) portion wise. The reaction mixture was stirred at rt overnight. Purification via a column chromatography afforded the title compound as a yellow oil (8.86 g, 51.4% yield). LCMS: rt=2.51 min, [M+H+]=316.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637536B2
Source datasetuspto-grants-2014_01
ORD IDord-5ec7bd81703e4a26b677f2cf9905f4ba
Source noteuspto-grants-2014_01