HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748067Generated: October 30, 2026
2-Ethylbutyraldehyde → HCID 68593352, compound
https://huagongshe.com/reaction/748067
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Ethylbutyraldehyde | HCID 7359 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Benzylimidazole | HCID 77918 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 68593352 | HCID 68593352 | 69% |
Reaction Steps
To a chilled reaction vessel at −45° C. containing 1-benzyl-1H-imidazole (3.0 g, 19.0 mmol) in Et2O (100 mL) was added a solution of n-butyllithium (2.5M in hexanes, 10.8 mL, 26.9 mmol) dropwise. After 30 min, the reaction vessel was cooled to −78° C. and 2-ethylbutyraldehyde (2.8 mL, 22.8 mmol) was added dropwise. The reaction mixture was warmed to 0° C. and stirred for 15 min, then poured into sat. aqueous NH4Cl and extracted with Et2O. The organic layer was washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The resulting yellow oil was purified by column chromatography (SiO2, EtOAc/hexane, 3:2, then 7:3) to yield a clear oil in 69% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07399778B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-22ef515c1a0e407fae3abea73fd0f058 |
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| Source note | uspto-grants-2008_07 |
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