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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269457Generated: October 31, 2026

Sodium borohydride → 3-{[(R)-1-(3,5-Difluorophenyl)ethylamino]-(4-fluorophenyl)methyl}phenylamine

https://huagongshe.com/reaction/2269457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantN-[(R)-1-(3,5-Difluorophenyl)ethyl]-N-[(4-fluorophenyl)-(3-nitrophenyl)methyl]amineHCID 70189758—
CatalystDichloronickel;hexahydrateHCID 11791229—
Product3-{[(R)-1-(3,5-Difluorophenyl)ethylamino]-(4-fluorophenyl)methyl}phenylamineHCID 70189768—

Reaction Steps

Following a reaction and purification procedure similar to those described in Example (59b), 4.40 g of N-[(R)-1-(3,5-difluorophenyl)ethyl]-N-[(4-fluorophenyl)-(3-nitrophenyl)methyl]amine [prepared as described in step (a) above], 6.54 g of nickel chloride hexahydrate and 1.81 g of sodium borohydride were reacted, to obtain 1.24 g of isomer A and 1.66 g of isomer B of the title compound as yellow oils, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329405B1
Source datasetuspto-grants-2001_12
ORD IDord-5cc33074077446558967c770e935ac58
Source noteuspto-grants-2001_12