HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109056Generated: October 31, 2026
N-butyl-8-(4,5-diphenyl-1H-imidazol-2-ylthio)octanamide → HCID 19021759, compound
https://huagongshe.com/reaction/1109056
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-butyl-8-(4,5-diphenyl-1H-imidazol-2-ylthio)octanamide | HCID 19021729 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19021759 | HCID 19021759 | 37% |
Reaction Steps
Part B. To a solution of lithium aluminum hydride (0.46 g, 0.012 mol) in dry tetrahydrofuran (15 mL) was added, dropwise, a solution of N-butyl-8-(4,5-diphenyl-1H-imidazol-2-ylthio)octanamide (1.20 g, 0.0027 mol) in tetrahydrofuran (8 mL) and the reaction mixture was stirred at reflux for 18 hours. The reaction mixture was cooled to 0° C. and quenched by the slow and careful sequential addition of water (0.46 mL), 15% sodium hydroxide (1.38 mL), and water (1.38 mL) and then the reaction mixture was stirred at 0° for 30 minutes. The solution was dried over magnesium sulfate and concentrated under vacuum, and the residue was chromatographed with 1:1 hexane-ethyl acetate and then with a gradient of 1:0 to 8:2 to 1:1 ethyl acetatemethanol. The resulting solid was triturated with hexane to give N-butyl-8-(4,5-diphenyl-1H-imidazol-2-ylthio)octanamine (0.45 g, 0.001 mol) as a white solid, mp 75°-78°. 1H NMR (CDCl3) δ 7.6-7.1 (m, 10H), 3.1(t,2H, J=7Hz), 2.5(t,2H, J=7Hz), 1.7-1.0(m, 16H), 0.9 (t, 3H, J=8Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05318984 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-85ba36ae532f4c0b84206e1017e5bc8b |
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| Source note | uspto-grants-1994_06 |
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