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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254417Generated: November 2, 2026

Sodium borohydride → HCID 19744522, compound

https://huagongshe.com/reaction/2254417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-(Thiophen-3-yl)benzaldehydeHCID 4547526—
ReactantHCID 19744585HCID 19744585—
ReactantDichloromethane methanolHCID 21226129—
SolventMethanolHCID 887—
ProductHCID 19744522HCID 1974452284%

Reaction Steps

65 mg of (E)-N-ethyl-N-(6-methoxy-6-methyl-2-hepten-4-ynyl)-3-aminobenzylamine and 43 mg of 3-(3thienyl)benzaldehyde were dissolved in 2 ml of methanol, and the solution was stirred overnight at room temperature. With stirring under ice cooling, 12.9 mg of sodium borohydride was added, and stirred for 1 hour at room temperature. The solvent was evaporated under reduced pressure, and the residue was dissolved in ethyl acetate and water. The organic layer was separated, and dried over anhydrous magnesium sulfate. The desiccant was separated by filtration, and the solvent was evaporated. The residue was purified by silica gel column chromatography Wakogel C-200, 5 g; eluting solvent: methylene chloride/ methanol=60/1] to give 87 mg (yield 84%) of the captioned compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05234946
Source datasetuspto-grants-1993_08
ORD IDord-83df4b4bd28a46fdad9216cdba7c3c28
Source noteuspto-grants-1993_08