HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323173Generated: October 30, 2026
Diisobutylaluminumhydride → HCID 22010670, compound
https://huagongshe.com/reaction/323173
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 22010702 | HCID 22010702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22010670 | HCID 22010670 | 97.5% |
Reaction Steps
To a solution of 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-(3-ethoxycarbonylprop-1-yloxy)phenyl]benzamide (1.10 g) in dichloromethane (20 ml) was added dropwise a solution of diisobutylaluminum hydride in toluene (1.5 M solution, 2 ml) at −78° C. and the mixture was stirred at the same temperature for 2 hours. The reaction was quenched with addition of water and the resulting mixture was warmed to ambient temperature. The mixture was extracted with dichloromethane and the organic phase was washed successively with 1N hydrochloric acid, water and brine. The organic solution was dried over magnesium sulfate and the solvent was evaporated in vacuo to give 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-(3-formylprop-1-yloxy)phenyl]benzamide (987 mg) as a syrup. The unstable aldehyde was immediately used for next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211242B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-a63bc6ff62534a929dfa3198dd730796 |
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| Source note | uspto-grants-2001_04 |
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