HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734902Generated: October 29, 2026
Allyl Alcohol → 3-(6-Isopropylaminopyridin-3-yl)propionaldehyde
https://huagongshe.com/reaction/734902
Participants
| Role | Name | HCID | Charge |
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| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-iodo-N-isopropylpyridin-2-amine | HCID 69058026 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-(6-Isopropylaminopyridin-3-yl)propionaldehyde | HCID 86076995 | — |
Reaction Steps
A mixture of 1.80 g (6.87 mmol) of (5-iodopyridin-2-yl)isopropylamine, 1.40 mL (10.7 mmol) of prop-2-en-1-ol, 1.39 g (16.49 mmol) of sodium hydrogen carbonate, 1.72 g (6.18 mmol) of tetrabutylammonium chloride, and 46 mg (0.20 mmol) of palladium (II) acetate in 10 mL of DMF was stirred under argon for 20 hours at 50° C. The reaction mixture was diluted with water and EtOAc, the organic phase was separated off, washed several times with water, and dried over magnesium sulfate. After the desiccant and solvent had been eliminated, the residue was purified by chromatography (silica gel, PE/EtOAc 1:1). Yield: 300 mg (23% of theoretical); ClIH16N2O (M=192.258); calc.: molpeak (M+H)+:193; found: molpeak (M+H)+:193; HPLC-MS: 3.58 minutes (method G).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07592358B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-4aefb381620f4cb9a07ccf2d2d9b5b7b |
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| Source note | uspto-grants-2009_09 |
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