HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478301Generated: October 27, 2026
Water → 2-(3-Methyl-4-chloro-pyridin-2-yl)-2-cyclopropyl-acetaldehyde
https://huagongshe.com/reaction/1478301
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Chloro-2-(1-cyclopropyl-2-methoxyvinyl)-3-methylpyridine | HCID 66980224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(3-Methyl-4-chloro-pyridin-2-yl)-2-cyclopropyl-acetaldehyde | HCID 18629355 | 67.8% |
Reaction Steps
To a solution of 4-chloro-2-(1-cyclopropyl-2-methoxyvinyl)-3-methylpyridine (1.7 g, 7.60 mmol) in THF (15 mL) a 2M aqueous solution of sulfuric acid (15.20 mL, 30.4 mmol) was added and the reaction mixture was stirred at 50° C. for a total of 2.5 h. The resulting mixture was poured into water and neutralized with a saturated sodium bicarbonate solution, and thereafter, extracted with chloroform (3×20 mL). The resulting organic layers were washed with saturated salt water (20 mL), dried over sodium sulfate and concentrated under reduced pressure. The resulting yellow solid was purified by silica gel column chromatography (hexane:ethyl acetate) (4:1) to obtain the aldehyde (1.08 g, 67.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09403818B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-6c91271efa8f4c36ace3e7919fcfdf19 |
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| Source note | uspto-grants-2016_08 |
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