HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257808Generated: November 1, 2026
Isopropanol → 1-Quinolin-6-ylcyclopropanecarbaldehyde
https://huagongshe.com/reaction/1257808
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | 1-(Quinolin-6-yl)cyclopropanecarbonitrile | HCID 66812840 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Quinolin-6-ylcyclopropanecarbaldehyde | HCID 59216277 | — |
Reaction Steps
Diisobutylaluminum hydride (1M in THF, 96 mL, 96 mmol) was added to a solution of 1-quinolin-6-ylcyclopropanecarbonitrile (12.4 g, 63.9 mmol) in toluene (120 mL) at −78° C. under an atmosphere of nitrogen. The reaction mixture was allowed to warm to −5 to 0° C., and stirred at that temperature for 3 h. The reaction mixture was cooled to −60° C. Isopropyl alcohol (10 mL) was carefully added dropwise. After stirring for 30 min, the reaction mixture was warmed to −5 to 0° C. The reaction mixture was diluted with ethyl acetate, quenched with water and extracted with ethyl acetate. The combined organic extracts were washed with water, brine, dried over sodium sulfate, filtered through a pad of silica gel eluting with 40% ethyl acetate in hexanes. The filtrate was concentrated to yield the desired product. (12 g, 95.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461330B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-ce3b2f4dfb364972b59643db8527eb72 |
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| Source note | uspto-grants-2013_06 |
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