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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269407Generated: October 30, 2026

Sodium borohydride → HCID 70188108, compound

https://huagongshe.com/reaction/2269407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 70188163HCID 70188163—
CatalystDichloronickel;hexahydrateHCID 11791229—
SolventMethanolHCID 887—
ProductHCID 70188108HCID 7018810829.3%

Reaction Steps

In a similar manner to that described in Example (1b), a solution of N-[(3-nitrophenyl)-(2-methoxyphenyl)methyl]-N-[(S)-1-(3-fluorophenyl)ethyl]amine (2.96 g) [prepared as described in step (a) above] in methanol (50 ml), nickel chloride hexahydrate (3.70 g) and sodium borohydride (1.24 g) were reacted, and the crude product was purified by reverse phase HPLC using a 40:60 by volume mixture of acetonitrile and an acetic acid buffer solution (water/acetic acid/triethylamine=1000:2:2) as the eluant, to afford isomer A of the title compound (540 mg) as a yellow oil and isomer B of the title compound (800 mg) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329405B1
Source datasetuspto-grants-2001_12
ORD IDord-fc458c2144bf484db6b7a6ae96781ac5
Source noteuspto-grants-2001_12