Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269397Generated: October 29, 2026

Sodium borohydride → HCID 70188144, compound

https://huagongshe.com/reaction/2269397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 70189816HCID 70189816—
CatalystDichloronickel;hexahydrateHCID 11791229—
SolventMethanolHCID 887—
ProductHCID 70188144HCID 70188144—

Reaction Steps

In a similar manner to that described in Example (1b), a solution of N-[(3-nitrophenyl)-(4-methoxyphenyl)methyl]-[(R)-1-(3,4-difluorophenyl)ethyl]amine (1.27 g) [prepared as described in step (a) above] in methanol (50 ml), nickel chloride hexahydrate (1.52 g) and sodium borohydride (510 mg) were reacted, and the reaction mixture was purified by chromatography through a silica gel column using a 1:8 by volume mixture of ethynyl acetate and toluene as the eluant, to afford isomer A (235 mg,) as a yellow oil and isomer B (240 mg) as a pale yellow oil of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329405B1
Source datasetuspto-grants-2001_12
ORD IDord-428a7a8cc8f74b27a8fc12dbb1e710d8
Source noteuspto-grants-2001_12