HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254417Generated: November 2, 2026
Sodium borohydride → HCID 19744522, compound
https://huagongshe.com/reaction/2254417
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-(Thiophen-3-yl)benzaldehyde | HCID 4547526 | — |
| Reactant | HCID 19744585 | HCID 19744585 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19744522 | HCID 19744522 | 84% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05234946 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-83df4b4bd28a46fdad9216cdba7c3c28 |
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| Source note | uspto-grants-1993_08 |
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