Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171450Generated: November 2, 2026

Borohydride → HCID 58828971, compound

https://huagongshe.com/reaction/1171450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorohydrideHCID 28123—
ReactantHCID 58828974HCID 58828974—
ReactantHCID 178442555HCID 178442555—
SolventTetrahydrofuran ethanolHCID 21873804—
ProductHCID 58828971HCID 58828971—

Reaction Steps

2.647 g (6.62 mmol, 3 eq) of resin-supported borohydride and 30 mg (0.06 mmol, 0.03 eq) of bis(bipyridine)dibromonickel (II) are added to a solution of 0.706 g (3.31 mmol, 1.5 eq) of 5-heptyl-4-methyl-4H-[1,2,4]-triazole-3-thiol in 10 ml of tetrahydrofuran/ethanol 5/5. To the suspension obtained there is added a solution of 100 mg (0.22 mmol, 1 eq) of ethyl [4-(4-iodo-2-propoxybenzylamino)phenyl]acetate in 10 ml of tetrahydrofuran/ethanol 5/5. The reaction mixture is stirred overnight under reflux. After returning to room temperature, the reaction medium is filtered, concentrated and then chromatographed on silica gel (heptane/ethyl acetate 40/60). After evaporation of the solvents, 0.750 g (63%) of the expected compound is recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829588B2
Source datasetuspto-grants-2010_11
ORD IDord-451756e1e3eb4ffaa47f27b4a5a7d69c
Source noteuspto-grants-2010_11