HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 578880Generated: November 2, 2026
Diisobutylaluminum hydride → HCID 89556341, compound
https://huagongshe.com/reaction/578880
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | HCID 89544502 | HCID 89544502 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 89556341 | HCID 89556341 | 97.2% |
Reaction Steps
1-(4,6-Dichloro-3-pyridyl)cyclopropanecarbonitrile (0.1 g, 0.469 mmol) was dissolved in Toluene (2.3 mL). At −10° C. DIBAL-H 1M in Toluene (0.98564 mL, 0.986 mmol) was added dropwise. The reaction mixture was stirred 30 min at −10° C. At −10° C. NaBH4 (0.10871 g, 2.816 mmol) was added, then carefully 3 mL MeOH. The reaction mixture was stirred 30 min at rt. It was poured into 25 ml of 1N potassium sodium tartrate. The pale yellow solution was extracted 3 times with Ether. The combined organic phases were washed with brine and dried with Na2SO4, filtrated and the filtrate evaporated. The product was obtained as a pale yellow oil (99 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040708B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-04d8bf1bce4d45f7b1e5d985f6d6de7d |
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| Source note | uspto-grants-2015_05 |
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