HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895835Generated: November 1, 2026
Ammonia;borane → 2-(Benzylsulfanyl)ethan-1-amine
https://huagongshe.com/reaction/1895835
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia;borane | HCID 419330 | — |
| Reactant | HCID 20488109 | HCID 20488109 | — |
| Catalyst | Cobalt(II) chloride | HCID 24288 | — |
| Catalyst | HCID 86652118 | HCID 86652118 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(Benzylsulfanyl)ethan-1-amine | HCID 31198 | — |
Reaction Steps
This compound was prepared in situ as described above. In a typical experiment, benzylthio ethanamine (0.2 g, 1.2 mmol) was dissolved in toluene (5 ml) and the solution was then added to a suspension of dichloro 1,5-cyclooctadiene ruthenium polymer [RuCl2(COD)]n in toluene (5 ml). The mixture was then stirred under argon at 100° C. for 2 hours. The solvent volume was reduced in vacuo to approximately 3 ml and a solid was precipitated by adding ether (10 ml) to obtain a reddish brown product. The activities of these catalysts are low for the hydrolysis of ammonia borane. The reactions with cobalt(II)chloride (CoCl2) and chlorobis(cyclooctene)iridium(I)dimer [IrCl(COE)2]2 were performed similarly. The three catalysts prepared in the section (section b) were all tested for ammonia borane hydrolysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518368B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-41cf2d2fd3e743dca3fb79c33df6c8ed |
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| Source note | uspto-grants-2013_08 |
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