HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823297Generated: November 1, 2026
Dimethylformamide → 3,5-Dichloropyridine-2-carbaldehyde
https://huagongshe.com/reaction/1823297
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dabco | HCID 9237 | — |
| Reactant | 3,5-Dichloropyridine | HCID 17153 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3,5-Dichloropyridine-2-carbaldehyde | HCID 22170168 | 49% |
Reaction Steps
Add a solution of n-butyl lithium (37.5 mL, 0.06 mol, 1.6 M in hexanes) to a mixture of 1,4-diazabicyclo-[2.2.2]octane (6.16 g, 0.055 mol) in diethyl ether (250 mL) at −10 to −20° C. under a nitrogen atmosphere. Stir for 45 min. and then cool to −70° C. Add 3,5-dichloropyridine (7.40 g, 0.05 mol) in small portions and stir for 1.5 h at this temperature. Add N,N-dimethylformamide (7.75 mL, 0.10 mol) dropwise via syringe and stir for 2 h and allow to slowly warm to ˜−20° C. Add water (200 mL) is added and extract with ethyl acetate. Dry over sodium sulfate and concentrate in vacuo. Elute over silica gel with hexanes/ethyl acetate to give the desired aldehyde (2.12 g, 49%) as a light yellowish solid. MS(ES): (M+1)+ 174.8, 175.8 m/z.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07037921B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-122bd88c9a59467b8a59342c25312dc0 |
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| Source note | uspto-grants-2006_05 |
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