HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411511Generated: October 30, 2026
Diisobutylaluminum hydride → HCID 23499479, compound
https://huagongshe.com/reaction/411511
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | HCID 23499480 | HCID 23499480 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23499479 | HCID 23499479 | — |
Reaction Steps
1-(2-(2,4-Difluorophenyl)ethyl]-4-(4-methoxycarbonylphenylsulphonyl)piperidine (0.6 g, 1.42 mmol) was dissolved in anhydrous CH2Cl2 (15 ml) and stirred under nitrogen at −78° C. DIBAL-H (1M in THF, 4.25 ml, 4.25 mmol) was added dropwise. The reaction mixture was stirred at −78° C. for 15 min, allowed to warm up to room temperature and stirred for 1 h. Crushed Na2SO4.10H2O (5 eq.) was added and the mixture left at room temperature overnight. Inorganic solid was filtered off and washed with CH2Cl2 and EtOAc. The organic filtrate was concentrated to give a beige solid. δH (360 MHz, CDCl3) 1.64-1.77 (2H, m), 1.94-2.06 (4H, m), 2.47-2.55 (2H, m), 2.70-2.76 (2H, m), 2.83-2.94 (2H, m), 3.02-3.08 (2H, m), 4.82 (2H, s), 6.71-6.82 (2H, m), 7.06-7.14 (1H, m), 7.55 (2H, d, 8 Hz), 7.85 (2H, d, 8 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06559166B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-53335cde408e4fd58048eaa24157201d |
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| Source note | uspto-grants-2003_05 |
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