HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250259Generated: October 30, 2026
HCID 21102222, compound → HCID 21102117, compound
https://huagongshe.com/reaction/2250259
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 21102222 | HCID 21102222 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 21102117 | HCID 21102117 | — |
Reaction Steps
Into a flame dried flask, N-(1-benzyl-piperidin-4-yl)-2-chloro-6-nitro-benzamide (1.67 g, 4.47 mmol) and lithium aluminium hydride (0.51 g, 13.43 mmol) were combined. To this was added anhydrous 1,4-dioxane (15 mL). The mixture was slowly brought to reflux and stirred for 16 h. The reaction mixture was cooled to 0° C. and excess lithium aluminium hydride destroyed by dropwise addition of methanol, followed by careful addition of 20% potassium hydroxide. The aluminum salts were filtered, the filtrate concentrated and used as is for the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07314883B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-af233b2945154ebaa2e9d79498ecaf7d |
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| Source note | uspto-grants-2008_01 |
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