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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269469Generated: November 1, 2026

Sodium borohydride → HCID 18334178, compound

https://huagongshe.com/reaction/2269469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 18334192HCID 18334192—
CatalystDichloronickel;hexahydrateHCID 11791229—
ProductHCID 18334178HCID 18334178—

Reaction Steps

Following a similar reaction, separation and purification procedure to that described in Example (59b), 2.41 of N-[(4-fluorophenyl)-(3-nitrophenyl)methyl]-N-[1-(thiophen-2-yl)ethyl]amine [prepared as described in step (a) above], 3.22 g of nickel chloride hexahydrate and 1.03 g of sodium borohydride were reacted, to obtain 687 mg of isomer A and 552 mg of isomer B of the title compound as pale yellow oils, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329405B1
Source datasetuspto-grants-2001_12
ORD IDord-88c472f48b4741aea7f423842d0ab01d
Source noteuspto-grants-2001_12