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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269403Generated: October 29, 2026

Sodium borohydride → 3-{(4-Fluorophenyl)-[1-(3,4-difluorophenyl)ethylamino]methyl}phenylamine

https://huagongshe.com/reaction/2269403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantN-[(3-Nitrophenyl)-(4-fluorophenyl)methyl]-N-[1-(3,4-difluorophenyl)ethyl]amineHCID 18334151—
CatalystDichloronickel;hexahydrateHCID 11791229—
SolventMethanolHCID 887—
Product3-{(4-Fluorophenyl)-[1-(3,4-difluorophenyl)ethylamino]methyl}phenylamineHCID 1833413321%

Reaction Steps

In a similar manner to that described in Example (15b), a solution of N-[(3-nitrophenyl)-(4-fluorophenyl)methyl]-N-[1-(3,4-difluorophenyl)ethyl]amine (3.0 g) [prepared as described in step (a) above] in methanol (10 ml), nickel chloride hexahydrate (3.69 g) and sodium borohydride (1.24 g) were reacted, and the reaction mixture was purified to afford isomer A of the title compound (630 mg) as a pale yellow oil and isomer B of the title compound (580 mg) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329405B1
Source datasetuspto-grants-2001_12
ORD IDord-45d96bbef1f64f888a119509ab1d9799
Source noteuspto-grants-2001_12